Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55764 |
| ensemblid | ENSG00000163913.14 |
| hgncid | 13556 |
| symbol | IFT122 |
| name | intraflagellar transport 122 |
| refseq_nuc | NM_052989.3 |
| refseq_prot | NP_443715.1 |
| ensembl_nuc | ENST00000348417.7 |
| ensembl_prot | ENSP00000324005.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 129440224 |
| end | 129520507 |
| strand | + |
| ver | v1.2 |
| region | chr3:129440224-129520507 |
| region5000 | chr3:129435224-129525507 |
| regionname0 | IFT122_chr3_129440224_129520507 |
| regionname5000 | IFT122_chr3_129435224_129525507 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1241 | 309 | 83 | 52 | 131 | 8 | 34 | 103 | IFT122_chr3_129435224_129525507 | IFT122 | MRAVL others(1236): Show |
chr3 | 129435224 | 129525507 |
| a0002 | 0/1 | 1241 | 31 | 9 | 5 | 9 | 2 | 5 | 4 | IFT122_chr3_129435224_129525507 | IFT122 | MRAVL others(1236): Show |
chr3 | 129435224 | 129525507 |
| a0003 | 0/0 | 1241 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | IFT122_chr3_129435224_129525507 | IFT122 | MRAVL others(1236): Show |
chr3 | 129435224 | 129525507 |
| a0004 | 0/0 | 1241 | 3 | 0 | 0 | 2 | 0 | 1 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | MRAVL others(1236): Show |
chr3 | 129435224 | 129525507 |
| a0005 | 0/0 | 1241 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | MRAVL others(1236): Show |
chr3 | 129435224 | 129525507 |
| a0006 | 0/0 | 1241 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | MRAVL others(1236): Show |
chr3 | 129435224 | 129525507 |
| a0007 | 0/0 | 1241 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | MRAVL others(1236): Show |
chr3 | 129435224 | 129525507 |
| a0008 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | MRAVL others(1236): Show |
chr3 | 129435224 | 129525507 |
| a0009 | 0/0 | 1241 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | MRAVL others(1236): Show |
chr3 | 129435224 | 129525507 |
| a0010 | 0/0 | 1241 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | MRAVL others(1236): Show |
chr3 | 129435224 | 129525507 |
| a0011 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | MRAVL others(1236): Show |
chr3 | 129435224 | 129525507 |
| a0012 | 0/0 | 1241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | MRAVL others(1236): Show |
chr3 | 129435224 | 129525507 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3723 | 282 | 67 | 48 | 125 | 7 | 34 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0001c0003 | 0/0 | 3723 | 6 | 6 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0001c0004 | 0/0 | 3723 | 6 | 3 | 2 | 0 | 1 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0001c0007 | 0/0 | 3723 | 3 | 1 | 2 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0001c0008 | 0/0 | 3723 | 3 | 0 | 0 | 3 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0001c0009 | 0/0 | 3723 | 2 | 2 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0001c0012 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0001c0015 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0001c0016 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0001c0019 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0001c0020 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0001c0022 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0001c0024 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0002c0002 | 0/1 | 3723 | 30 | 9 | 5 | 8 | 2 | 5 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0002c0013 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0003c0005 | 0/0 | 3723 | 5 | 0 | 0 | 5 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0004c0006 | 0/0 | 3723 | 3 | 0 | 0 | 2 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0005c0025 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0006c0010 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0007c0014 | 0/0 | 3723 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0008c0011 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0009c0021 | 0/0 | 3723 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0010c0018 | 0/0 | 3723 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0011c0023 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 | ||
| a0012c0017 | 0/0 | 3723 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | ATGAG others(3718): Show |
chr3 | 129435224 | 129525507 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4075 | 281 | 66 | 48 | 125 | 7 | 34 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0001t0002 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0003t0001 | 0/0 | 4075 | 6 | 6 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0004t0001 | 0/0 | 4075 | 6 | 3 | 2 | 0 | 1 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0007t0001 | 0/0 | 4075 | 3 | 1 | 2 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0008t0001 | 0/0 | 4075 | 3 | 0 | 0 | 3 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0009t0001 | 0/0 | 4075 | 2 | 2 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0012t0001 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0015t0001 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0016t0001 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0019t0001 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0020t0001 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0022t0001 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0001c0024t0001 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0002c0002t0001 | 0/1 | 4075 | 30 | 9 | 5 | 8 | 2 | 5 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0002c0013t0001 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0003c0005t0001 | 0/0 | 4075 | 5 | 0 | 0 | 5 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0004c0006t0001 | 0/0 | 4075 | 3 | 0 | 0 | 2 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0005c0025t0001 | 0/0 | 4075 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0006c0010t0001 | 0/0 | 4075 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0007c0014t0001 | 0/0 | 4075 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0008c0011t0001 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0009c0021t0001 | 0/0 | 4075 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0010c0018t0001 | 0/0 | 4075 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0011c0023t0001 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| a0012c0017t0001 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | AACGC others(4070): Show |
chr3 | 129435224 | 129525507 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0014 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0003t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0004t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0004t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0004t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0007t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0007t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0007t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0008t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0008t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0008t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0009t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0009t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0012t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0015t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0016t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0019t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0020t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0022t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0001c0024t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0300 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0002c0013t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0003c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0003c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0003c0005t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0003c0005t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0003c0005t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0004c0006t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0004c0006t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0004c0006t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0005c0025t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0006c0010t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0007c0014t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0008c0011t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0009c0021t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0010c0018t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0011c0023t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| a0012c0017t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0327 | EUR | GBR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00408 | hp2 | a0002 | c0013 | t0001 | g0305 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | CHS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0021 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0315 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0304 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01109 | hp2 | a0005 | c0025 | t0001 | g0187 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0308 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01175 | hp1 | a0006 | c0010 | t0001 | g0193 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01175 | hp2 | a0001 | c0007 | t0001 | g0330 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01361 | hp1 | a0001 | c0004 | t0001 | g0021 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01433 | hp1 | a0007 | c0014 | t0001 | g0314 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0020 | EUR | IBS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0020 | EUR | IBS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | IBS | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01884 | hp2 | a0001 | c0004 | t0001 | g0323 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0299 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02015 | hp2 | a0008 | c0011 | t0001 | g0073 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02083 | hp1 | a0004 | c0006 | t0001 | g0286 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02129 | hp2 | a0003 | c0005 | t0001 | g0131 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02145 | hp1 | a0001 | c0004 | t0001 | g0326 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0322 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02258 | hp1 | a0001 | c0007 | t0001 | g0329 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02280 | hp1 | a0001 | c0009 | t0001 | g0100 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0274 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0269 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0272 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02723 | hp1 | a0001 | c0020 | t0001 | g0260 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0270 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02886 | hp1 | a0001 | c0016 | t0001 | g0149 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0316 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0310 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02976 | hp1 | a0001 | c0012 | t0001 | g0268 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03195 | hp1 | a0001 | c0015 | t0001 | g0026 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0273 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0302 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0311 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0313 | SAS | STU | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03704 | hp1 | a0009 | c0021 | t0001 | g0205 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03834 | hp1 | a0004 | c0006 | t0001 | g0324 | SAS | BEB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0309 | SAS | BEB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03927 | hp2 | a0010 | c0018 | t0001 | g0238 | SAS | BEB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | BEB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | STU | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | STU | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0301 | SAS | STU | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | STU | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0303 | SAS | STU | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | CHB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18747 | hp2 | a0001 | c0024 | t0001 | g0241 | EAS | CHB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0319 | AFR | YRI | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18940 | hp2 | a0001 | c0022 | t0001 | g0251 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18942 | hp2 | a0001 | c0008 | t0001 | g0092 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18943 | hp1 | a0004 | c0006 | t0001 | g0285 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18966 | hp1 | a0003 | c0005 | t0001 | g0157 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18984 | hp1 | a0001 | c0008 | t0001 | g0072 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18987 | hp2 | a0011 | c0023 | t0001 | g0069 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18994 | hp2 | a0001 | c0008 | t0001 | g0068 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19000 | hp2 | a0012 | c0017 | t0001 | g0114 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19030 | hp1 | a0001 | c0009 | t0001 | g0099 | AFR | LWK | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | LWK | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19055 | hp2 | a0003 | c0005 | t0001 | g0132 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19056 | hp2 | a0001 | c0019 | t0001 | g0075 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19058 | hp1 | a0003 | c0005 | t0001 | g0152 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19084 | hp2 | a0003 | c0005 | t0001 | g0134 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | YRI | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | YRI | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ASW | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | TSI | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | GIH | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | GIH | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01123 | hp1 | a0001 | c0007 | t0001 | g0328 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0271 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | USA | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | USA | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | USA | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0300 | REF | REF | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0014 | REF | REF | IFT122_chr3_129435224_129525507 | IFT122 | chr3 | 129435224 | 129525507 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129458604 | C | T | 1 | a0005 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.199C>T | p.Arg67Cys | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/30 | 306/4075 | 199/3726 | 67/1241 | chr3 | 129458604 | |||
| chr3:129458619 | T | G | 1 | a0006 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.214T>G | p.Ser72Ala | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/30 | 321/4075 | 214/3726 | 72/1241 | chr3 | 129458619 | |||
| chr3:129461259 | A | C | 1 | a0005 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.304A>C | p.Asn102His | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/30 | 411/4075 | 304/3726 | 102/1241 | chr3 | 129461259 | |||
| chr3:129476323 | G | T | 1 | a0003 | 5 | HG02129.hp2 NA18966.hp1 NA19055.hp2 others(2): Show |
missense_variant | MODERATE | c.825G>T | p.Lys275Asn | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 10/30 | 932/4075 | 825/3726 | 275/1241 | chr3 | 129476323 | |||
| chr3:129476328 | G | A | 1 | a0008 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.830G>A | p.Arg277Gln | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 10/30 | 937/4075 | 830/3726 | 277/1241 | chr3 | 129476328 | |||
| chr3:129476757 | G | A | 1 | a0004 | 3 | HG02083.hp1 HG03834.hp1 NA18943.hp1 |
missense_variant | MODERATE | c.1103G>A | p.Ser368Asn | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/30 | 1210/4075 | 1103/3726 | 368/1241 | chr3 | 129476757 | |||
| chr3:129488348 | A | C | 1 | a0009 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.1943A>C | p.Glu648Ala | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/30 | 2050/4075 | 1943/3726 | 648/1241 | chr3 | 129488348 | |||
| chr3:129495459 | G | A | 2 | a0002 a0007 |
31 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(28): Show |
missense_variant | MODERATE | c.2060G>A | p.Arg687Gln | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/30 | 2167/4075 | 2060/3726 | 687/1241 | chr3 | 129495459 | |||
| chr3:129499992 | G | A | 1 | a0007 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.2299G>A | p.Ala767Thr | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/30 | 2406/4075 | 2299/3726 | 767/1241 | chr3 | 129499992 | |||
| chr3:129506507 | T | G | 1 | a0005 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.2749T>G | p.Tyr917Asp | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 22/30 | 2856/4075 | 2749/3726 | 917/1241 | chr3 | 129506507 | |||
| chr3:129514391 | A | G | 1 | a0011 | 1 | NA18987.hp2 | missense_variant&splice_region_variant | MODERATE | c.2990A>G | p.Lys997Arg | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/30 | 3097/4075 | 2990/3726 | 997/1241 | chr3 | 129514391 | |||
| chr3:129517586 | C | G | 1 | a0010 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.3383C>G | p.Ala1128Gly | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/30 | 3490/4075 | 3383/3726 | 1128/1241 | chr3 | 129517586 | |||
| chr3:129519629 | G | A | 1 | a0012 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.3533G>A | p.Arg1178His | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 29/30 | 3640/4075 | 3533/3726 | 1178/1241 | chr3 | 129519629 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129466932 | C | T | 1 | a0001c0024 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.606C>T | p.Ala202Ala | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/30 | 713/4075 | 606/3726 | 202/1241 | chr3 | 129466932 | |||
| chr3:129476680 | C | T | 2 | a0001c0008 a0011c0023 |
4 | NA18942.hp2 NA18984.hp1 NA18987.hp2 others(1): Show |
synonymous_variant | LOW | c.1026C>T | p.Asp342Asp | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/30 | 1133/4075 | 1026/3726 | 342/1241 | chr3 | 129476680 | |||
| chr3:129478107 | G | A | 1 | a0001c0012 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1239G>A | p.Glu413Glu | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/30 | 1346/4075 | 1239/3726 | 413/1241 | chr3 | 129478107 | |||
| chr3:129481574 | G | A | 1 | a0002c0013 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.1533G>A | p.Leu511Leu | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/30 | 1640/4075 | 1533/3726 | 511/1241 | chr3 | 129481574 | |||
| chr3:129483544 | G | T | 2 | a0001c0004 a0001c0007 |
9 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
synonymous_variant | LOW | c.1713G>T | p.Ser571Ser | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/30 | 1820/4075 | 1713/3726 | 571/1241 | chr3 | 129483544 | |||
| chr3:129488259 | C | T | 2 | a0001c0009 a0001c0022 |
3 | HG02280.hp1 NA18940.hp2 NA19030.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1854C>T | p.Ser618Ser | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/30 | 1961/4075 | 1854/3726 | 618/1241 | chr3 | 129488259 | |||
| chr3:129488313 | T | C | 1 | a0001c0012 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1908T>C | p.Ile636Ile | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/30 | 2015/4075 | 1908/3726 | 636/1241 | chr3 | 129488313 | |||
| chr3:129495553 | C | T | 1 | a0001c0003 | 6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
synonymous_variant | LOW | c.2154C>T | p.His718His | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/30 | 2261/4075 | 2154/3726 | 718/1241 | chr3 | 129495553 | |||
| chr3:129500042 | C | A | 1 | a0001c0012 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.2349C>A | p.Ile783Ile | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/30 | 2456/4075 | 2349/3726 | 783/1241 | chr3 | 129500042 | |||
| chr3:129502750 | C | T | 1 | a0001c0003 | 6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
synonymous_variant | LOW | c.2415C>T | p.Arg805Arg | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 20/30 | 2522/4075 | 2415/3726 | 805/1241 | chr3 | 129502750 | |||
| chr3:129502768 | C | T | 1 | a0001c0020 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.2433C>T | p.Cys811Cys | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 20/30 | 2540/4075 | 2433/3726 | 811/1241 | chr3 | 129502768 | |||
| chr3:129502789 | G | A | 1 | a0001c0015 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2454G>A | p.Leu818Leu | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 20/30 | 2561/4075 | 2454/3726 | 818/1241 | chr3 | 129502789 | |||
| chr3:129504396 | C | T | 1 | a0001c0019 | 1 | NA19056.hp2 | synonymous_variant | LOW | c.2625C>T | p.Asn875Asn | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/30 | 2732/4075 | 2625/3726 | 875/1241 | chr3 | 129504396 | |||
| chr3:129506440 | G | A | 1 | a0001c0009 | 2 | HG02280.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.2682G>A | p.Ala894Ala | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 22/30 | 2789/4075 | 2682/3726 | 894/1241 | chr3 | 129506440 | |||
| chr3:129517506 | G | T | 1 | a0001c0012 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.3303G>T | p.Gly1101Gly | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/30 | 3410/4075 | 3303/3726 | 1101/1241 | chr3 | 129517506 | |||
| chr3:129519147 | C | T | 1 | a0001c0007 | 3 | HG01123.hp1 HG01175.hp2 HG02258.hp1 |
synonymous_variant | LOW | c.3432C>T | p.Ile1144Ile | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 28/30 | 3539/4075 | 3432/3726 | 1144/1241 | chr3 | 129519147 | |||
| chr3:129519177 | G | A | 1 | a0001c0016 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.3462G>A | p.Leu1154Leu | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 28/30 | 3569/4075 | 3462/3726 | 1154/1241 | chr3 | 129519177 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129520369 | T | G | 1 | a0001c0001t0002 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*104T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 30/30 | 104 | chr3 | 129520369 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129440598 | G | T | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | NA18987.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.41+227G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129440598 | |||||||
| chr3:129440786 | A | G | 6 | a0001c0004t0001g0021 a0001c0004t0001g0326 a0001c0004t0001g0327 others(3): Show |
7 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.41+415A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129440786 | |||||||
| chr3:129440823 | C | T | 1 | a0001c0001t0001g0325 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.41+452C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129440823 | |||||||
| chr3:129440835 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.41+464A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129440835 | |||||||
| chr3:129440996 | A | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0275 others(66): Show |
79 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.41+625A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129440996 | |||||||
| chr3:129441000 | T | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.41+629T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129441000 | |||||||
| chr3:129441101 | C | T | 9 | a0001c0001t0001g0259 a0001c0001t0001g0261 a0001c0001t0001g0262 others(6): Show |
9 | HG02559.hp1 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.41+730C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129441101 | |||||||
| chr3:129441186 | T | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.41+815T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129441186 | |||||||
| chr3:129441292 | C | T | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.41+921C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129441292 | |||||||
| chr3:129441351 | G | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.41+980G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129441351 | |||||||
| chr3:129441375 | T | G | 1 | a0001c0001t0001g0034 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.41+1004T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129441375 | |||||||
| chr3:129441438 | G | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.41+1067G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129441438 | |||||||
| chr3:129441944 | G | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.41+1573G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129441944 | |||||||
| chr3:129442061 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.41+1690G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129442061 | |||||||
| chr3:129442080 | A | T | 1 | a0004c0006t0001g0324 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.41+1709A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129442080 | |||||||
| chr3:129442145 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
248 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.41+1774G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129442145 | |||||||
| chr3:129442242 | A | AT | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.41+1877dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 129442242 | ||||||
| chr3:129442413 | C | T | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
65 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.41+2042C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129442413 | |||||||
| chr3:129442427 | G | T | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+2056G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129442427 | |||||||
| chr3:129442579 | C | CA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(83): Show |
93 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.41+2220dupA | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 129442579 | ||||||
| chr3:129442581 | A | AC | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.41+2210_41+2211ins others(1): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129442581 | |||||||
| chr3:129442582 | A | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(11): Show |
15 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.41+2211A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129442582 | |||||||
| chr3:129442622 | A | G | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.41+2251A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129442622 | |||||||
| chr3:129442636 | C | T | 8 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(5): Show |
9 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.41+2265C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129442636 | |||||||
| chr3:129443092 | A | C | 25 | a0002c0002t0001g0003 a0002c0002t0001g0017 a0002c0002t0001g0018 others(22): Show |
31 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.41+2721A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129443092 | |||||||
| chr3:129443092 | A | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(27): Show |
33 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.41+2721A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129443092 | |||||||
| chr3:129443114 | A | G | 2 | a0001c0004t0001g0322 a0001c0004t0001g0323 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.41+2743A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129443114 | |||||||
| chr3:129443249 | A | C | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.41+2878A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129443249 | |||||||
| chr3:129443415 | A | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.41+3044A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129443415 | |||||||
| chr3:129443526 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0001g0116 |
4 | HG02258.hp2 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+3155T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129443526 | |||||||
| chr3:129443533 | G | A | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.41+3162G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129443533 | |||||||
| chr3:129443649 | T | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.41+3278T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129443649 | |||||||
| chr3:129443658 | G | A | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.41+3287G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129443658 | |||||||
| chr3:129443707 | AAAG | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0287 a0001c0001t0001g0288 others(5): Show |
10 | HG01255.hp1 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.41+3341_41+3343del others(3): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 129443707 | ||||||
| chr3:129444198 | C | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG00639.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.41+3827C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129444198 | |||||||
| chr3:129444212 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.41+3841C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129444212 | |||||||
| chr3:129444259 | G | T | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.41+3888G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129444259 | |||||||
| chr3:129444309 | G | A | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.41+3938G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129444309 | |||||||
| chr3:129444371 | T | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+4000T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129444371 | |||||||
| chr3:129444377 | C | G | 1 | a0001c0001t0001g0295 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.41+4006C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129444377 | |||||||
| chr3:129444386 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.41+4015C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129444386 | |||||||
| chr3:129444604 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41+4233C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129444604 | |||||||
| chr3:129444789 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.41+4418A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129444789 | |||||||
| chr3:129444800 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+4429G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129444800 | |||||||
| chr3:129444886 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.41+4515T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129444886 | |||||||
| chr3:129445274 | C | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0002g0036 |
3 | HG01243.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.42-4597C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129445274 | |||||||
| chr3:129445325 | C | CA | 19 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(16): Show |
21 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.42-4538dupA | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 129445325 | ||||||
| chr3:129445392 | C | T | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.42-4479C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129445392 | |||||||
| chr3:129445595 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-4276A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129445595 | |||||||
| chr3:129445655 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG01496.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.42-4216C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129445655 | |||||||
| chr3:129445856 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.42-4015C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129445856 | |||||||
| chr3:129446023 | A | C | 1 | a0004c0006t0001g0286 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.42-3848A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446023 | |||||||
| chr3:129446093 | TATG | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
20 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.42-3775_42-3773del others(3): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 129446093 | ||||||
| chr3:129446125 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.42-3746C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446125 | |||||||
| chr3:129446157 | A | G | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.42-3714A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446157 | |||||||
| chr3:129446198 | G | A | 2 | a0002c0002t0001g0003 a0002c0002t0001g0299 |
4 | HG01891.hp2 HG02451.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-3673G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446198 | |||||||
| chr3:129446228 | G | GT | 6 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0258 others(3): Show |
6 | HG01243.hp2 HG01517.hp2 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-3631dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 129446228 | ||||||
| chr3:129446374 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.42-3497G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446374 | |||||||
| chr3:129446390 | A | AATTTTTT others(2): Show |
55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.42-3479_42-3471dup others(9): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 129446390 | ||||||
| chr3:129446405 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0116 |
3 | HG02258.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.42-3466C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446405 | |||||||
| chr3:129446406 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.42-3465G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446406 | |||||||
| chr3:129446514 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
92 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.42-3357C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446514 | |||||||
| chr3:129446578 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
171 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.42-3293A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446578 | |||||||
| chr3:129446680 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
92 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.42-3191C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446680 | |||||||
| chr3:129446704 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
92 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.42-3167G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446704 | |||||||
| chr3:129446903 | A | G | 1 | a0002c0002t0001g0319 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.42-2968A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446903 | |||||||
| chr3:129446929 | T | C | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.42-2942T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446929 | |||||||
| chr3:129446965 | A | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0002g0036 |
3 | HG01243.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.42-2906A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129446965 | |||||||
| chr3:129447415 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
93 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.42-2456A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129447415 | |||||||
| chr3:129447434 | A | G | 14 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(11): Show |
15 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.42-2437A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129447434 | |||||||
| chr3:129447475 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.42-2396G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129447475 | |||||||
| chr3:129447581 | C | T | 25 | a0002c0002t0001g0003 a0002c0002t0001g0017 a0002c0002t0001g0018 others(22): Show |
31 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.42-2290C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129447581 | |||||||
| chr3:129447607 | G | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-2264G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129447607 | |||||||
| chr3:129447657 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.42-2214C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129447657 | |||||||
| chr3:129447661 | C | T | 1 | a0001c0009t0001g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.42-2210C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129447661 | |||||||
| chr3:129447725 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.42-2146C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129447725 | |||||||
| chr3:129447747 | G | A | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-2124G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129447747 | |||||||
| chr3:129447757 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.42-2114C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129447757 | |||||||
| chr3:129447965 | T | TG | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
75 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.42-1899dupG | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 129447965 | ||||||
| chr3:129448223 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.42-1648T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448223 | |||||||
| chr3:129448247 | C | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-1624C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448247 | |||||||
| chr3:129448266 | C | T | 4 | a0001c0012t0001g0268 a0004c0006t0001g0285 a0004c0006t0001g0286 others(1): Show |
4 | HG02083.hp1 HG02976.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-1605C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448266 | |||||||
| chr3:129448400 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
237 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.42-1471A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448400 | |||||||
| chr3:129448529 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.42-1342G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448529 | |||||||
| chr3:129448564 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.42-1307G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448564 | |||||||
| chr3:129448587 | C | A | 1 | a0001c0001t0001g0296 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.42-1284C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448587 | |||||||
| chr3:129448696 | T | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG01109.hp1 HG03209.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-1175T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448696 | |||||||
| chr3:129448697 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.42-1174A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448697 | |||||||
| chr3:129448697 | AT | A | 37 | a0001c0001t0001g0148 a0001c0001t0001g0196 a0001c0001t0001g0320 others(34): Show |
44 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.42-1162delT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 129448697 | ||||||
| chr3:129448701 | T | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
122 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.42-1170T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448701 | |||||||
| chr3:129448809 | A | C | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-1062A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448809 | |||||||
| chr3:129448817 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG03490.hp2 HG03492.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.42-1054G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448817 | |||||||
| chr3:129448952 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.42-919G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129448952 | |||||||
| chr3:129449014 | A | G | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.42-857A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129449014 | |||||||
| chr3:129449065 | C | A | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.42-806C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129449065 | |||||||
| chr3:129449143 | T | C | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-728T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129449143 | |||||||
| chr3:129449255 | T | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.42-616T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129449255 | |||||||
| chr3:129449453 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.42-418G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129449453 | |||||||
| chr3:129449595 | C | A | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.42-276C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129449595 | |||||||
| chr3:129449606 | T | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(51): Show |
63 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.42-265T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129449606 | |||||||
| chr3:129449617 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.42-254A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129449617 | |||||||
| chr3:129449641 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0002g0036 |
3 | HG01243.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.42-230G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129449641 | |||||||
| chr3:129449726 | T | A | 1 | a0001c0001t0001g0005 | 2 | HG01070.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.42-145T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129449726 | |||||||
| chr3:129449806 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | NA18943.hp2 NA19076.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.42-65C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129449806 | |||||||
| chr3:129449811 | C | G | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG00609.hp1 NA18947.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-60C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 1/29 | chr3 | 129449811 | |||||||
| chr3:129450011 | CT | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0120 others(23): Show |
28 | HG00735.hp1 HG01255.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.108+89delT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr3 | 129450011 | ||||||
| chr3:129450011 | CTT | C | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.108+88_108+89delTT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr3 | 129450011 | ||||||
| chr3:129450101 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.108+164G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450101 | |||||||
| chr3:129450333 | C | G | 1 | a0003c0005t0001g0157 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.108+396C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450333 | |||||||
| chr3:129450386 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.108+449C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450386 | |||||||
| chr3:129450450 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0173 |
3 | HG02602.hp2 HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.108+513G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450450 | |||||||
| chr3:129450612 | AATCCAAA others(6): Show |
A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.108+676_108+688del others(13): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450612 | |||||||
| chr3:129450713 | G | GT | 41 | a0001c0001t0001g0034 a0001c0001t0001g0107 a0001c0001t0001g0108 others(38): Show |
41 | HG00423.hp2 HG01169.hp2 HG01975.hp2 others(38): Show |
intron_variant | MODIFIER | c.108+800dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr3 | 129450713 | ||||||
| chr3:129450732 | TTTTTTG | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(47): Show |
59 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.108+796_108+801del others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450732 | |||||||
| chr3:129450736 | TTG | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(17): Show |
20 | HG00738.hp1 HG01167.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.108+800_108+801del others(2): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450736 | |||||||
| chr3:129450737 | TG | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
58 | HG00544.hp1 HG00597.hp1 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.108+802delG | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr3 | 129450737 | ||||||
| chr3:129450738 | G | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0041 others(25): Show |
29 | HG00558.hp2 HG01891.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.108+801G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450738 | |||||||
| chr3:129450783 | C | T | 36 | a0001c0001t0001g0150 a0001c0001t0001g0320 a0001c0001t0001g0321 others(33): Show |
43 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.108+846C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450783 | |||||||
| chr3:129450790 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.108+853G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450790 | |||||||
| chr3:129450802 | G | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.108+865G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450802 | |||||||
| chr3:129450813 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
92 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.108+876C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450813 | |||||||
| chr3:129450872 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0245 |
2 | HG02293.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.108+935C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450872 | |||||||
| chr3:129450877 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | NA18968.hp1 NA18975.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.108+940C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450877 | |||||||
| chr3:129450911 | G | A | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.108+974G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450911 | |||||||
| chr3:129450921 | C | T | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.108+984C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450921 | |||||||
| chr3:129450971 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0275 |
2 | HG03516.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.109-943C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450971 | |||||||
| chr3:129450975 | C | T | 1 | a0001c0008t0001g0092 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.109-939C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129450975 | |||||||
| chr3:129451099 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.109-815G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451099 | |||||||
| chr3:129451135 | G | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0001g0116 |
4 | HG02258.hp2 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-779G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451135 | |||||||
| chr3:129451275 | TTTTTTAT others(9): Show |
T | 8 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(5): Show |
9 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.109-627_109-612del others(16): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr3 | 129451275 | ||||||
| chr3:129451277 | T | A | 1 | a0012c0017t0001g0114 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.109-637T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451277 | |||||||
| chr3:129451291 | A | T | 1 | a0001c0016t0001g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.109-623A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451291 | |||||||
| chr3:129451356 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.109-558C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451356 | |||||||
| chr3:129451362 | A | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(10): Show |
15 | HG00597.hp1 HG01081.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.109-552A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451362 | |||||||
| chr3:129451369 | C | T | 1 | a0002c0002t0001g0020 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.109-545C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451369 | |||||||
| chr3:129451370 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
172 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.109-544A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451370 | |||||||
| chr3:129451393 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.109-521G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451393 | |||||||
| chr3:129451462 | C | T | 51 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0167 others(48): Show |
52 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.109-452C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451462 | |||||||
| chr3:129451489 | G | A | 1 | a0001c0020t0001g0260 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.109-425G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451489 | |||||||
| chr3:129451571 | T | A | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.109-343T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451571 | |||||||
| chr3:129451691 | G | A | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.109-223G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451691 | |||||||
| chr3:129451899 | T | C | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.109-15T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 2/29 | chr3 | 129451899 | |||||||
| chr3:129452274 | G | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG01884.hp1 HG02809.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.193+276G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452274 | |||||||
| chr3:129452341 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.193+343T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452341 | |||||||
| chr3:129452376 | G | A | 60 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(57): Show |
64 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.193+378G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452376 | |||||||
| chr3:129452407 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.193+409A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452407 | |||||||
| chr3:129452551 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.193+553T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452551 | |||||||
| chr3:129452573 | G | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | NA18999.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.193+575G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452573 | |||||||
| chr3:129452679 | A | G | 9 | a0001c0001t0001g0162 a0001c0001t0001g0168 a0001c0001t0001g0198 others(6): Show |
9 | HG01167.hp2 HG01258.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.193+681A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452679 | |||||||
| chr3:129452785 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.193+787G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452785 | |||||||
| chr3:129452843 | CAG | C | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG03239.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.193+846_193+847del others(2): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452843 | |||||||
| chr3:129452859 | C | T | 1 | a0002c0002t0001g0316 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.193+861C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452859 | |||||||
| chr3:129452871 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.193+873T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452871 | |||||||
| chr3:129452959 | G | T | 1 | a0001c0009t0001g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.193+961G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452959 | |||||||
| chr3:129452966 | A | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0102 a0001c0001t0001g0103 others(7): Show |
11 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.193+968A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129452966 | |||||||
| chr3:129453014 | GC | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.193+1024delC | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129453014 | ||||||
| chr3:129453021 | C | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+1023C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453021 | |||||||
| chr3:129453023 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
93 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.193+1025A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453023 | |||||||
| chr3:129453060 | G | A | 6 | a0001c0004t0001g0021 a0001c0004t0001g0326 a0001c0004t0001g0327 others(3): Show |
7 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+1062G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453060 | |||||||
| chr3:129453119 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.193+1121G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453119 | |||||||
| chr3:129453280 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.193+1282A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453280 | |||||||
| chr3:129453311 | A | G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.193+1313A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453311 | |||||||
| chr3:129453332 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.193+1334G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453332 | |||||||
| chr3:129453402 | T | C | 3 | a0001c0004t0001g0021 a0001c0004t0001g0326 a0001c0004t0001g0327 |
4 | HG00140.hp1 HG00738.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+1404T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453402 | |||||||
| chr3:129453551 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.193+1553C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453551 | |||||||
| chr3:129453654 | T | C | 32 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0117 others(29): Show |
34 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.193+1656T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453654 | |||||||
| chr3:129453854 | A | AC | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.193+1856_193+1857i others(3): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453854 | |||||||
| chr3:129453865 | G | T | 2 | a0001c0001t0001g0265 a0001c0001t0001g0267 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.193+1867G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453865 | |||||||
| chr3:129453918 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.193+1920C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129453918 | |||||||
| chr3:129454210 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
172 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.193+2212T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454210 | |||||||
| chr3:129454212 | C | G | 1 | a0001c0001t0001g0229 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.193+2214C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454212 | |||||||
| chr3:129454379 | G | C | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.193+2381G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454379 | |||||||
| chr3:129454395 | T | TA | 10 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0121 others(7): Show |
10 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.193+2413dupA | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454395 | ||||||
| chr3:129454395 | TA | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0101 others(19): Show |
23 | HG01070.hp1 HG01109.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.193+2413delA | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454395 | ||||||
| chr3:129454508 | CATAT | C | 6 | a0001c0001t0001g0284 a0001c0001t0001g0288 a0001c0001t0001g0290 others(3): Show |
6 | HG02135.hp1 HG02559.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+2511_193+2514d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454508 | |||||||
| chr3:129454508 | CATATTT | C | 5 | a0001c0001t0001g0283 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG02083.hp1 HG03491.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+2511_193+2516d others(8): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454508 | |||||||
| chr3:129454508 | CATATTTG others(3): Show |
C | 1 | a0001c0001t0001g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.193+2511_193+2520d others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454508 | |||||||
| chr3:129454509 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0287 others(1): Show |
6 | HG01255.hp1 HG02055.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+2511A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454509 | |||||||
| chr3:129454511 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.193+2514_193+2515i others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454511 | ||||||
| chr3:129454511 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0287 others(2): Show |
7 | HG01255.hp1 HG02055.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+2513A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454511 | |||||||
| chr3:129454513 | T | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0281 others(9): Show |
14 | HG01255.hp1 HG02055.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.193+2515T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454513 | |||||||
| chr3:129454513 | T | TGTGTGTG others(4): Show |
2 | a0001c0001t0002g0036 a0002c0002t0001g0301 |
2 | HG02486.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.193+2515_193+2516i others(13): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454513 | |||||||
| chr3:129454513 | T | TGTGTGTG others(8): Show |
2 | a0001c0001t0001g0122 a0001c0001t0001g0151 |
2 | NA19000.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.193+2515_193+2516i others(17): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454513 | |||||||
| chr3:129454513 | T | TTG | 33 | a0001c0001t0001g0015 a0001c0001t0001g0123 a0001c0001t0001g0141 others(30): Show |
34 | HG00609.hp1 HG00609.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.193+2558_193+2559d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTGTG | 35 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0115 others(32): Show |
38 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.193+2556_193+2559d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTGTGTG | 15 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0121 others(12): Show |
17 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.193+2554_193+2559d others(8): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTGTGTGT others(1): Show |
29 | a0001c0001t0001g0010 a0001c0001t0001g0101 a0001c0001t0001g0117 others(26): Show |
32 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.193+2552_193+2559d others(10): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTGTGTGT others(3): Show |
13 | a0001c0001t0001g0038 a0001c0001t0001g0102 a0001c0001t0001g0103 others(10): Show |
15 | HG01496.hp1 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.193+2550_193+2559d others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTGTGTGT others(5): Show |
8 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0109 others(5): Show |
9 | HG01175.hp2 HG02071.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.193+2548_193+2559d others(14): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTGTGTGT others(7): Show |
6 | a0001c0001t0001g0008 a0001c0001t0001g0139 a0001c0001t0001g0261 others(3): Show |
7 | HG01433.hp1 HG02258.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+2546_193+2559d others(16): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTGTGTGT others(9): Show |
2 | a0001c0001t0001g0105 a0001c0012t0001g0268 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.193+2544_193+2559d others(18): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTGTGTGT others(11): Show |
1 | a0001c0001t0001g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.193+2542_193+2559d others(20): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTGTGTGT others(13): Show |
2 | a0001c0001t0001g0106 a0001c0001t0001g0325 |
2 | HG03225.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.193+2540_193+2559d others(22): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTGTGTGT others(15): Show |
1 | a0001c0001t0001g0140 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.193+2538_193+2559d others(24): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTTGTGTG others(4): Show |
1 | a0001c0001t0001g0047 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.193+2516_193+2517i others(13): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTTTGTG | 7 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0078 others(4): Show |
7 | HG00544.hp1 NA18943.hp2 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+2516_193+2517i others(8): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTTTGTGT others(1): Show |
7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02071.hp1 HG02132.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+2516_193+2517i others(10): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTTTGTGT others(3): Show |
29 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(26): Show |
34 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.193+2516_193+2517i others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTTTGTGT others(5): Show |
11 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
11 | HG01346.hp1 NA18612.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.193+2516_193+2517i others(14): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTTTGTGT others(7): Show |
6 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0094 others(3): Show |
6 | HG02015.hp2 NA18942.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+2516_193+2517i others(16): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTTTGTGT others(9): Show |
1 | a0001c0001t0001g0095 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.193+2516_193+2517i others(18): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | T | TTTTGTGT others(11): Show |
1 | a0001c0001t0001g0077 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.193+2516_193+2517i others(20): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | TTG | T | 16 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(13): Show |
16 | HG01884.hp1 HG02109.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.193+2558_193+2559d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | TTGTG | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0173 others(3): Show |
7 | HG02602.hp2 HG03704.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.193+2556_193+2559d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | TTGTGTGT others(5): Show |
T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): Show |
13 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.193+2548_193+2559d others(14): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454513 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0001g0202 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.193+2546_193+2559d others(16): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129454513 | ||||||
| chr3:129454517 | G | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG01884.hp1 HG02809.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.193+2519G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454517 | |||||||
| chr3:129454519 | G | T | 1 | a0001c0001t0001g0048 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.193+2521G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454519 | |||||||
| chr3:129454527 | G | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(9): Show |
13 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.193+2529G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454527 | |||||||
| chr3:129454559 | A | G | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.193+2561A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454559 | |||||||
| chr3:129454802 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
92 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.193+2804C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454802 | |||||||
| chr3:129454857 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.193+2859C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454857 | |||||||
| chr3:129454909 | C | T | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.193+2911C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129454909 | |||||||
| chr3:129455164 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.193+3166C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129455164 | |||||||
| chr3:129455213 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0283 others(14): Show |
19 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.193+3215C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129455213 | |||||||
| chr3:129455234 | G | A | 3 | a0001c0004t0001g0021 a0001c0004t0001g0326 a0001c0004t0001g0327 |
4 | HG00140.hp1 HG00738.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.193+3236G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129455234 | |||||||
| chr3:129455236 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.193+3238G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129455236 | |||||||
| chr3:129455247 | A | T | 4 | a0002c0002t0001g0003 a0002c0002t0001g0299 a0002c0002t0001g0310 others(1): Show |
6 | HG01891.hp2 HG02451.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.193+3249A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129455247 | |||||||
| chr3:129455300 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.194-3299G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129455300 | |||||||
| chr3:129455329 | T | C | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.194-3270T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129455329 | |||||||
| chr3:129455388 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(153): Show |
172 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.194-3211A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129455388 | |||||||
| chr3:129455425 | C | A | 1 | a0001c0001t0001g0255 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.194-3174C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129455425 | |||||||
| chr3:129455451 | G | A | 2 | a0001c0004t0001g0322 a0001c0004t0001g0323 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.194-3148G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129455451 | |||||||
| chr3:129455717 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.194-2882G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129455717 | |||||||
| chr3:129455898 | TGAG | T | 31 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0101 others(28): Show |
33 | HG01069.hp2 HG01071.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.194-2674_194-2672d others(5): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129455898 | ||||||
| chr3:129455898 | TGAGGAG | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(82): Show |
96 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.194-2677_194-2672d others(8): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129455898 | ||||||
| chr3:129455934 | A | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.194-2665A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129455934 | |||||||
| chr3:129456419 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.194-2180A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129456419 | |||||||
| chr3:129456501 | G | GT | 63 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
67 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.194-2097dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129456501 | ||||||
| chr3:129456568 | C | T | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.194-2031C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129456568 | |||||||
| chr3:129456574 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.194-2025T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129456574 | |||||||
| chr3:129456830 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.194-1769C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129456830 | |||||||
| chr3:129456871 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.194-1728G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129456871 | |||||||
| chr3:129457129 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.194-1470A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129457129 | |||||||
| chr3:129457131 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.194-1468C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129457131 | |||||||
| chr3:129457235 | T | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0325 |
2 | NA18612.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.194-1364T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129457235 | |||||||
| chr3:129457358 | C | T | 1 | a0002c0002t0001g0020 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.194-1241C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129457358 | |||||||
| chr3:129457535 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.194-1064G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129457535 | |||||||
| chr3:129457607 | C | T | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG01496.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.194-992C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129457607 | |||||||
| chr3:129457629 | G | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.194-970G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129457629 | |||||||
| chr3:129457730 | T | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-869T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129457730 | |||||||
| chr3:129457732 | G | GT | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
142 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.194-846dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129457732 | ||||||
| chr3:129457732 | G | GTT | 9 | a0001c0001t0001g0045 a0001c0001t0001g0070 a0001c0001t0001g0078 others(6): Show |
9 | HG02280.hp2 HG04204.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-847_194-846dup others(2): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129457732 | ||||||
| chr3:129457732 | G | GTTT | 5 | a0001c0004t0001g0021 a0001c0004t0001g0323 a0001c0004t0001g0327 others(2): Show |
6 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.194-848_194-846dup others(3): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr3 | 129457732 | ||||||
| chr3:129457738 | T | TG | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | NA18943.hp2 NA19076.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.194-861_194-860ins others(1): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129457738 | |||||||
| chr3:129457797 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.194-802G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129457797 | |||||||
| chr3:129457798 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
171 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.194-801T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129457798 | |||||||
| chr3:129458120 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.194-479A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129458120 | |||||||
| chr3:129458306 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG01255.hp2 HG01975.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.194-293C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129458306 | |||||||
| chr3:129458503 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.194-96C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 3/29 | chr3 | 129458503 | |||||||
| chr3:129458805 | G | T | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.272+128G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129458805 | |||||||
| chr3:129459066 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.272+389C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459066 | |||||||
| chr3:129459088 | A | G | 9 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0001g0284 others(6): Show |
9 | HG02083.hp1 HG02135.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.272+411A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459088 | |||||||
| chr3:129459283 | TTTTTG | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.272+627_272+631del others(5): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459283 | ||||||
| chr3:129459352 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.272+675C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459352 | |||||||
| chr3:129459391 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.272+714G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459391 | |||||||
| chr3:129459435 | G | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.272+758G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459435 | |||||||
| chr3:129459445 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.272+768A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459445 | |||||||
| chr3:129459542 | C | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.272+865C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459542 | |||||||
| chr3:129459609 | T | TTTCC | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 others(1): Show |
4 | HG03654.hp2 NA18995.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.272+957_272+960dup others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459609 | ||||||
| chr3:129459609 | T | TTTCCTTC others(5): Show |
1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.272+949_272+960dup others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459609 | ||||||
| chr3:129459609 | TTTCC | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(112): Show |
128 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.272+957_272+960del others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459609 | ||||||
| chr3:129459652 | TCTTC | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0278 others(2): Show |
6 | HG01891.hp1 HG02896.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.272+989_272+992del others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459652 | ||||||
| chr3:129459666 | T | C | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0276 others(1): Show |
4 | HG01884.hp1 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.272+989T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459666 | |||||||
| chr3:129459680 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.272+1003C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459680 | |||||||
| chr3:129459682 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.272+1005C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459682 | |||||||
| chr3:129459684 | T | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.272+1007T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459684 | |||||||
| chr3:129459684 | T | TCTTC | 6 | a0001c0001t0001g0065 a0001c0001t0001g0239 a0001c0001t0001g0245 others(3): Show |
6 | HG01975.hp1 HG02109.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.272+1049_272+1052d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459684 | ||||||
| chr3:129459684 | TCTTC | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
128 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.272+1049_272+1052d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459684 | ||||||
| chr3:129459684 | TCTTCCTT others(1): Show |
T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(63): Show |
73 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.272+1045_272+1052d others(10): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459684 | ||||||
| chr3:129459684 | TCTTCCTT others(5): Show |
T | 63 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
66 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.272+1041_272+1052d others(14): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459684 | ||||||
| chr3:129459684 | TCTTCCTT others(9): Show |
T | 2 | a0001c0001t0001g0008 a0001c0012t0001g0268 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.272+1037_272+1052d others(18): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459684 | ||||||
| chr3:129459691 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.272+1014T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459691 | |||||||
| chr3:129459722 | T | TTCCC | 3 | a0001c0007t0001g0328 a0001c0007t0001g0329 a0001c0007t0001g0330 |
3 | HG01123.hp1 HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.272+1048_272+1049i others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459722 | ||||||
| chr3:129459726 | T | C | 37 | a0001c0001t0001g0106 a0001c0001t0001g0168 a0001c0001t0001g0256 others(34): Show |
44 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.272+1049T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459726 | |||||||
| chr3:129459730 | C | T | 2 | a0001c0001t0001g0240 a0001c0003t0001g0273 |
2 | HG01993.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.272+1053C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459730 | |||||||
| chr3:129459740 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0168 |
2 | HG03225.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.272+1063C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459740 | |||||||
| chr3:129459742 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0168 |
2 | HG03225.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.272+1065C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459742 | |||||||
| chr3:129459744 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0168 |
2 | HG03225.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.272+1067T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459744 | |||||||
| chr3:129459744 | TCTTC | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
215 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.272+1095_272+1098d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459744 | ||||||
| chr3:129459748 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.272+1071C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459748 | |||||||
| chr3:129459750 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.272+1073T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459750 | |||||||
| chr3:129459752 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.272+1075C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459752 | |||||||
| chr3:129459760 | CCTTCCTT others(9): Show |
C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.272+1087_272+1102d others(18): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129459760 | ||||||
| chr3:129459792 | C | G | 1 | a0002c0002t0001g0303 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.272+1115C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459792 | |||||||
| chr3:129459888 | G | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.272+1211G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459888 | |||||||
| chr3:129459996 | C | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.273-1232C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129459996 | |||||||
| chr3:129460025 | C | T | 21 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0019 others(18): Show |
25 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.273-1203C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129460025 | |||||||
| chr3:129460041 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.273-1187C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129460041 | |||||||
| chr3:129460439 | TC | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.273-788delC | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129460439 | |||||||
| chr3:129460446 | TA | T | 8 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(5): Show |
9 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.273-781delA | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129460446 | |||||||
| chr3:129460447 | A | AT | 21 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0281 others(18): Show |
23 | HG00735.hp1 HG01081.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.273-779dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129460447 | ||||||
| chr3:129460450 | A | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
163 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.273-778A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129460450 | |||||||
| chr3:129460534 | A | G | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.273-694A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129460534 | |||||||
| chr3:129460552 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.273-676G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129460552 | |||||||
| chr3:129460780 | C | CTG | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.273-448_273-447ins others(2): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129460780 | |||||||
| chr3:129460808 | AT | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.273-417delT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 129460808 | ||||||
| chr3:129460897 | C | A | 1 | a0001c0001t0001g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.273-331C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129460897 | |||||||
| chr3:129460955 | G | T | 1 | a0001c0001t0001g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.273-273G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129460955 | |||||||
| chr3:129460956 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.273-272T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129460956 | |||||||
| chr3:129461118 | G | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.273-110G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129461118 | |||||||
| chr3:129461201 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.273-27A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 4/29 | chr3 | 129461201 | |||||||
| chr3:129461578 | G | T | 1 | a0001c0001t0001g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.349+274G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129461578 | |||||||
| chr3:129461660 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.349+356C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129461660 | |||||||
| chr3:129461746 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
248 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.349+442G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129461746 | |||||||
| chr3:129461965 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.349+661C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129461965 | |||||||
| chr3:129462035 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.349+731G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129462035 | |||||||
| chr3:129462037 | G | A | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.349+733G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129462037 | |||||||
| chr3:129462280 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.349+976T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129462280 | |||||||
| chr3:129462303 | A | T | 1 | a0001c0001t0001g0146 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.349+999A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129462303 | |||||||
| chr3:129462624 | G | C | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.350-936G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129462624 | |||||||
| chr3:129462652 | A | G | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.350-908A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129462652 | |||||||
| chr3:129462659 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.350-901G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129462659 | |||||||
| chr3:129462926 | GCAT | G | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-630_350-628del others(3): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr3 | 129462926 | ||||||
| chr3:129462938 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.350-622T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129462938 | |||||||
| chr3:129463219 | T | A | 1 | a0002c0002t0001g0303 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.350-341T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129463219 | |||||||
| chr3:129463247 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.350-313G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129463247 | |||||||
| chr3:129463263 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.350-297A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129463263 | |||||||
| chr3:129463332 | A | G | 1 | a0002c0002t0001g0019 | 2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.350-228A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 5/29 | chr3 | 129463332 | |||||||
| chr3:129463745 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.416+119T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 6/29 | chr3 | 129463745 | |||||||
| chr3:129463924 | T | C | 4 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG01081.hp1 HG01346.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.416+298T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 6/29 | chr3 | 129463924 | |||||||
| chr3:129464059 | G | C | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.416+433G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 6/29 | chr3 | 129464059 | |||||||
| chr3:129464129 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.416+503C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 6/29 | chr3 | 129464129 | |||||||
| chr3:129464192 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.417-443T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 6/29 | chr3 | 129464192 | |||||||
| chr3:129464377 | A | AG | 5 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG01109.hp1 HG03209.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.417-256dupG | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr3 | 129464377 | ||||||
| chr3:129464382 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.417-253T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 6/29 | chr3 | 129464382 | |||||||
| chr3:129464499 | G | A | 1 | a0001c0007t0001g0328 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.417-136G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 6/29 | chr3 | 129464499 | |||||||
| chr3:129464560 | G | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.417-75G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 6/29 | chr3 | 129464560 | |||||||
| chr3:129465060 | C | T | 8 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(5): Show |
9 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.563+279C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465060 | |||||||
| chr3:129465100 | T | G | 1 | a0001c0001t0001g0170 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.563+319T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465100 | |||||||
| chr3:129465114 | A | AGT | 7 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0192 others(4): Show |
7 | HG01168.hp2 HG01169.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.563+379_563+380dup others(2): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | A | AGTGT | 3 | a0001c0001t0001g0195 a0001c0001t0001g0256 a0010c0018t0001g0238 |
3 | HG03239.hp2 HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.563+377_563+380dup others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | AGT | A | 18 | a0001c0001t0001g0142 a0001c0001t0001g0165 a0001c0001t0001g0169 others(15): Show |
18 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.563+379_563+380del others(2): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | AGTGT | A | 27 | a0001c0001t0001g0035 a0001c0001t0001g0115 a0001c0001t0001g0120 others(24): Show |
27 | HG00140.hp2 HG01074.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.563+377_563+380del others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | AGTGTGT | A | 62 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
67 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.563+375_563+380del others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | AGTGTGTG others(1): Show |
A | 21 | a0001c0001t0001g0034 a0001c0001t0001g0119 a0001c0001t0001g0130 others(18): Show |
21 | HG00423.hp2 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.563+373_563+380del others(8): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | AGTGTGTG others(3): Show |
A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0124 a0001c0001t0001g0128 others(5): Show |
9 | HG02602.hp2 HG02723.hp1 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.563+371_563+380del others(10): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | AGTGTGTG others(5): Show |
A | 36 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0001t0001g0052 others(33): Show |
37 | HG00558.hp2 HG00735.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.563+369_563+380del others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | AGTGTGTG others(7): Show |
A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(66): Show |
74 | HG00544.hp1 HG00597.hp1 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.563+367_563+380del others(14): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | AGTGTGTG others(9): Show |
A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0080 others(9): Show |
15 | HG01255.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.563+365_563+380del others(16): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | AGTGTGTG others(11): Show |
A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0054 a0001c0001t0001g0281 others(18): Show |
24 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.563+363_563+380del others(18): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | AGTGTGTG others(13): Show |
A | 21 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0002c0002t0001g0003 others(18): Show |
25 | HG00408.hp2 HG00642.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.563+361_563+380del others(20): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | AGTGTGTG others(15): Show |
A | 8 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(5): Show |
9 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.563+359_563+380del others(22): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465114 | AGTGTGTG others(17): Show |
A | 1 | a0002c0002t0001g0316 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.563+357_563+380del others(24): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465114 | ||||||
| chr3:129465125 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.563+344G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465125 | |||||||
| chr3:129465158 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.563+377T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465158 | |||||||
| chr3:129465339 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.563+558A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465339 | |||||||
| chr3:129465465 | C | CT | 17 | a0001c0001t0001g0086 a0001c0001t0001g0091 a0001c0001t0001g0102 others(14): Show |
17 | HG01074.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.563+707dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465465 | ||||||
| chr3:129465465 | CT | C | 87 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
91 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.563+707delT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465465 | ||||||
| chr3:129465465 | CTT | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0040 others(48): Show |
60 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.563+706_563+707del others(2): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465465 | ||||||
| chr3:129465465 | CTTT | C | 8 | a0001c0001t0001g0294 a0001c0001t0001g0298 a0002c0002t0001g0301 others(5): Show |
8 | HG01070.hp1 HG01168.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.563+705_563+707del others(3): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465465 | ||||||
| chr3:129465497 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.563+716G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465497 | |||||||
| chr3:129465505 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.563+724C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465505 | |||||||
| chr3:129465539 | C | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.563+758C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465539 | |||||||
| chr3:129465539 | C | T | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.563+758C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465539 | |||||||
| chr3:129465571 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.563+790C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465571 | |||||||
| chr3:129465624 | CCACGCCT others(303): Show |
C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
171 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.563+863_564-937del | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465624 | ||||||
| chr3:129465637 | A | AT | 17 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0110 others(14): Show |
17 | HG01167.hp2 HG01175.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.563+872dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465637 | ||||||
| chr3:129465683 | C | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.563+902C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465683 | |||||||
| chr3:129465727 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.563+946C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465727 | |||||||
| chr3:129465893 | C | T | 1 | a0009c0021t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.564-997C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465893 | |||||||
| chr3:129465965 | A | T | 1 | a0001c0001t0001g0090 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.564-925A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129465965 | |||||||
| chr3:129465974 | A | AT | 5 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG01109.hp1 HG03209.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.564-910dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129465974 | ||||||
| chr3:129466023 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.564-867G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129466023 | |||||||
| chr3:129466101 | G | A | 2 | a0001c0004t0001g0322 a0001c0004t0001g0323 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.564-789G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129466101 | |||||||
| chr3:129466366 | G | A | 1 | a0001c0003t0001g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.564-524G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129466366 | |||||||
| chr3:129466495 | C | CT | 15 | a0001c0001t0001g0034 a0001c0001t0001g0102 a0001c0001t0001g0104 others(12): Show |
15 | HG02135.hp2 HG02145.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.564-371dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129466495 | ||||||
| chr3:129466495 | CT | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
78 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.564-371delT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129466495 | ||||||
| chr3:129466495 | CTT | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(29): Show |
34 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.564-372_564-371del others(2): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129466495 | ||||||
| chr3:129466495 | CTTTTTTT others(6): Show |
C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.564-383_564-371del others(13): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 129466495 | ||||||
| chr3:129466798 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
248 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.564-92T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 7/29 | chr3 | 129466798 | |||||||
| chr3:129467081 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.740+15G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129467081 | |||||||
| chr3:129467298 | CT | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.740+236delT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr3 | 129467298 | ||||||
| chr3:129467427 | G | A | 27 | a0001c0001t0001g0013 a0001c0001t0001g0162 a0001c0001t0001g0168 others(24): Show |
28 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.740+361G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129467427 | |||||||
| chr3:129467457 | C | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.740+391C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129467457 | |||||||
| chr3:129467831 | C | A | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.740+765C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129467831 | |||||||
| chr3:129467958 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.740+892A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129467958 | |||||||
| chr3:129468113 | C | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.740+1047C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129468113 | |||||||
| chr3:129468176 | C | T | 1 | a0002c0002t0001g0017 | 2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.740+1110C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129468176 | |||||||
| chr3:129468358 | T | G | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.741-984T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129468358 | |||||||
| chr3:129468360 | T | G | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.741-982T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129468360 | |||||||
| chr3:129468378 | C | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.741-964C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129468378 | |||||||
| chr3:129468434 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.741-908C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129468434 | |||||||
| chr3:129468437 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.741-905G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129468437 | |||||||
| chr3:129468488 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.741-854A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129468488 | |||||||
| chr3:129468835 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.741-507C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129468835 | |||||||
| chr3:129468870 | A | G | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
65 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.741-472A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129468870 | |||||||
| chr3:129468896 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.741-446C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129468896 | |||||||
| chr3:129469119 | C | G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.741-223C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129469119 | |||||||
| chr3:129469137 | C | G | 1 | a0002c0002t0001g0309 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.741-205C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129469137 | |||||||
| chr3:129469144 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.741-198G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129469144 | |||||||
| chr3:129469180 | T | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.741-162T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129469180 | |||||||
| chr3:129469229 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.741-113A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129469229 | |||||||
| chr3:129469237 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
92 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.741-105C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 8/29 | chr3 | 129469237 | |||||||
| chr3:129469482 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
236 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.816+65G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129469482 | |||||||
| chr3:129469716 | T | TAGGA | 4 | a0001c0001t0001g0225 a0001c0001t0001g0232 a0001c0001t0001g0239 others(1): Show |
4 | HG02293.hp1 HG02293.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+299_816+300ins others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129469716 | |||||||
| chr3:129469803 | T | G | 2 | a0002c0002t0001g0317 a0002c0002t0001g0318 |
2 | HG00621.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.816+386T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129469803 | |||||||
| chr3:129469832 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.816+415C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129469832 | |||||||
| chr3:129469913 | A | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0002g0036 |
3 | HG01243.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.816+496A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129469913 | |||||||
| chr3:129470054 | C | T | 1 | a0001c0007t0001g0328 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.816+637C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129470054 | |||||||
| chr3:129470238 | TTTTA | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(51): Show |
63 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.816+849_816+852del others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr3 | 129470238 | ||||||
| chr3:129470364 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.816+947C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129470364 | |||||||
| chr3:129470458 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.816+1041G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129470458 | |||||||
| chr3:129470459 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.816+1042G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129470459 | |||||||
| chr3:129470490 | C | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.816+1073C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129470490 | |||||||
| chr3:129470500 | C | T | 3 | a0001c0004t0001g0021 a0001c0004t0001g0326 a0001c0004t0001g0327 |
4 | HG00140.hp1 HG00738.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+1083C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129470500 | |||||||
| chr3:129470511 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.816+1094C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129470511 | |||||||
| chr3:129470592 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.816+1175A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129470592 | |||||||
| chr3:129470618 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.816+1201T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129470618 | |||||||
| chr3:129470761 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
20 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.816+1344G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129470761 | |||||||
| chr3:129471077 | T | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.816+1660T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129471077 | |||||||
| chr3:129471081 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG01496.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.816+1664G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129471081 | |||||||
| chr3:129471087 | G | A | 2 | a0001c0001t0001g0261 a0001c0020t0001g0260 |
2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.816+1670G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129471087 | |||||||
| chr3:129471158 | G | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.816+1741G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129471158 | |||||||
| chr3:129471360 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.816+1943A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129471360 | |||||||
| chr3:129471439 | T | C | 1 | a0002c0002t0001g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.816+2022T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129471439 | |||||||
| chr3:129471451 | C | CTG | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.816+2038_816+2039d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr3 | 129471451 | ||||||
| chr3:129471470 | T | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.816+2053T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129471470 | |||||||
| chr3:129471539 | T | C | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | NA18943.hp2 NA19076.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.816+2122T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129471539 | |||||||
| chr3:129471874 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
92 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.816+2457C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129471874 | |||||||
| chr3:129471918 | A | C | 1 | a0001c0003t0001g0271 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.816+2501A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129471918 | |||||||
| chr3:129471963 | T | C | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+2546T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129471963 | |||||||
| chr3:129472037 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.816+2620C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129472037 | |||||||
| chr3:129472043 | T | TCC | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.816+2627_816+2628d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr3 | 129472043 | ||||||
| chr3:129472108 | C | G | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.816+2691C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129472108 | |||||||
| chr3:129472143 | T | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.816+2726T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129472143 | |||||||
| chr3:129472267 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.816+2850C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129472267 | |||||||
| chr3:129472333 | A | T | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.816+2916A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129472333 | |||||||
| chr3:129472474 | T | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
20 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.816+3057T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129472474 | |||||||
| chr3:129472591 | T | G | 1 | a0002c0002t0001g0311 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.816+3174T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129472591 | |||||||
| chr3:129472725 | GT | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
92 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.816+3310delT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr3 | 129472725 | ||||||
| chr3:129472791 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.816+3374C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129472791 | |||||||
| chr3:129472815 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.816+3398T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129472815 | |||||||
| chr3:129472991 | T | C | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.817-3324T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129472991 | |||||||
| chr3:129473141 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0071 |
3 | NA18960.hp2 NA18973.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.817-3174C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129473141 | |||||||
| chr3:129473172 | G | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.817-3143G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129473172 | |||||||
| chr3:129473204 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.817-3111G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129473204 | |||||||
| chr3:129473246 | A | C | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-3069A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129473246 | |||||||
| chr3:129473585 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-2730A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129473585 | |||||||
| chr3:129473667 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.817-2648G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129473667 | |||||||
| chr3:129473697 | C | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-2618C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129473697 | |||||||
| chr3:129473726 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.817-2589G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129473726 | |||||||
| chr3:129473811 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.817-2504A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129473811 | |||||||
| chr3:129473903 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.817-2412A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129473903 | |||||||
| chr3:129473931 | CT | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
171 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.817-2381delT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr3 | 129473931 | ||||||
| chr3:129473967 | C | A | 1 | a0001c0022t0001g0251 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.817-2348C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129473967 | |||||||
| chr3:129473994 | T | C | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-2321T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129473994 | |||||||
| chr3:129474013 | T | G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.817-2302T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129474013 | |||||||
| chr3:129474067 | C | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
171 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.817-2248C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129474067 | |||||||
| chr3:129474104 | A | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0109 |
2 | HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.817-2211A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129474104 | |||||||
| chr3:129474500 | A | G | 1 | a0002c0002t0001g0299 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.817-1815A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129474500 | |||||||
| chr3:129474600 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
92 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.817-1715C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129474600 | |||||||
| chr3:129474851 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.817-1464A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129474851 | |||||||
| chr3:129475151 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.817-1164A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129475151 | |||||||
| chr3:129475487 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.817-828G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129475487 | |||||||
| chr3:129475513 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.817-802G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129475513 | |||||||
| chr3:129475606 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
171 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.817-709G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129475606 | |||||||
| chr3:129475621 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.817-694C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129475621 | |||||||
| chr3:129475675 | A | G | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.817-640A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129475675 | |||||||
| chr3:129475681 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.817-634G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129475681 | |||||||
| chr3:129475762 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.817-553C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129475762 | |||||||
| chr3:129475952 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.817-363T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129475952 | |||||||
| chr3:129475971 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.817-344A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129475971 | |||||||
| chr3:129476020 | C | G | 1 | a0001c0001t0001g0031 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.817-295C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129476020 | |||||||
| chr3:129476097 | T | G | 25 | a0002c0002t0001g0003 a0002c0002t0001g0017 a0002c0002t0001g0018 others(22): Show |
31 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.817-218T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129476097 | |||||||
| chr3:129476128 | A | G | 25 | a0002c0002t0001g0003 a0002c0002t0001g0017 a0002c0002t0001g0018 others(22): Show |
31 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.817-187A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129476128 | |||||||
| chr3:129476143 | C | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-172C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129476143 | |||||||
| chr3:129476193 | T | C | 1 | a0002c0002t0001g0319 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.817-122T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 9/29 | chr3 | 129476193 | |||||||
| chr3:129476820 | C | T | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
65 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1147+19C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | chr3 | 129476820 | |||||||
| chr3:129476833 | G | A | 4 | a0002c0002t0001g0003 a0002c0002t0001g0299 a0002c0002t0001g0310 others(1): Show |
6 | HG01891.hp2 HG02451.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1147+32G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | chr3 | 129476833 | |||||||
| chr3:129476834 | ACAGGTGG others(3): Show |
A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1147+43_1147+52del others(10): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr3 | 129476834 | ||||||
| chr3:129476864 | A | T | 1 | a0001c0001t0001g0325 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1147+63A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | chr3 | 129476864 | |||||||
| chr3:129476920 | A | T | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1147+119A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | chr3 | 129476920 | |||||||
| chr3:129476940 | G | GT | 43 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(40): Show |
51 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1147+143dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr3 | 129476940 | ||||||
| chr3:129476940 | G | GTT | 8 | a0001c0004t0001g0021 a0001c0004t0001g0323 a0001c0004t0001g0327 others(5): Show |
9 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1147+142_1147+143d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr3 | 129476940 | ||||||
| chr3:129476945 | C | CT | 8 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1147+160dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr3 | 129476945 | ||||||
| chr3:129476945 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1147+144C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | chr3 | 129476945 | |||||||
| chr3:129476945 | CTTTTTT | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1147+155_1147+160d others(8): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr3 | 129476945 | ||||||
| chr3:129477145 | C | A | 25 | a0002c0002t0001g0003 a0002c0002t0001g0017 a0002c0002t0001g0018 others(22): Show |
31 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1147+344C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | chr3 | 129477145 | |||||||
| chr3:129477278 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1147+477A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | chr3 | 129477278 | |||||||
| chr3:129477552 | A | T | 25 | a0002c0002t0001g0003 a0002c0002t0001g0017 a0002c0002t0001g0018 others(22): Show |
31 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1148-464A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | chr3 | 129477552 | |||||||
| chr3:129477704 | T | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
20 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.1148-312T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 11/29 | chr3 | 129477704 | |||||||
| chr3:129478265 | TC | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1350+55delC | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 129478265 | ||||||
| chr3:129478271 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1350+53C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129478271 | |||||||
| chr3:129478272 | C | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
92 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1350+54C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129478272 | |||||||
| chr3:129478433 | G | GTTTTA | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1350+223_1350+227d others(7): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 129478433 | ||||||
| chr3:129478480 | G | A | 2 | a0001c0008t0001g0072 a0001c0008t0001g0092 |
2 | NA18942.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1350+262G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129478480 | |||||||
| chr3:129478557 | C | T | 1 | a0006c0010t0001g0193 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1350+339C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129478557 | |||||||
| chr3:129478602 | A | G | 32 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0117 others(29): Show |
34 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1350+384A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129478602 | |||||||
| chr3:129478660 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1350+442C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129478660 | |||||||
| chr3:129478673 | T | C | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1350+455T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129478673 | |||||||
| chr3:129478836 | A | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1350+618A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129478836 | |||||||
| chr3:129478969 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1350+751C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129478969 | |||||||
| chr3:129479009 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1351-776A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129479009 | |||||||
| chr3:129479048 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1351-737A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129479048 | |||||||
| chr3:129479088 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0213 |
2 | NA18944.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1351-697G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129479088 | |||||||
| chr3:129479212 | A | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1351-573A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129479212 | |||||||
| chr3:129479247 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1351-538A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129479247 | |||||||
| chr3:129479255 | C | CA | 24 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0048 others(21): Show |
25 | HG01069.hp1 HG01175.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.1351-506dupA | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 129479255 | ||||||
| chr3:129479255 | CA | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0022 others(80): Show |
93 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1351-506delA | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 129479255 | ||||||
| chr3:129479255 | CAA | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0104 others(11): Show |
16 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1351-507_1351-506d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 129479255 | ||||||
| chr3:129479350 | T | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1351-435T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129479350 | |||||||
| chr3:129479473 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1351-312C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129479473 | |||||||
| chr3:129479566 | G | T | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1351-219G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129479566 | |||||||
| chr3:129479625 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1351-160T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129479625 | |||||||
| chr3:129479709 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1351-76C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 12/29 | chr3 | 129479709 | |||||||
| chr3:129479951 | G | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0287 a0001c0001t0001g0288 others(5): Show |
10 | HG01255.hp1 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1488+29G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 13/29 | chr3 | 129479951 | |||||||
| chr3:129480030 | C | T | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1488+108C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 13/29 | chr3 | 129480030 | |||||||
| chr3:129480372 | G | T | 1 | a0001c0001t0001g0048 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1488+450G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 13/29 | chr3 | 129480372 | |||||||
| chr3:129480838 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1489-692T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 13/29 | chr3 | 129480838 | |||||||
| chr3:129480933 | T | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1489-597T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 13/29 | chr3 | 129480933 | |||||||
| chr3:129480998 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0215 |
3 | NA19066.hp2 NA19074.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1489-532G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 13/29 | chr3 | 129480998 | |||||||
| chr3:129481072 | A | T | 2 | a0001c0001t0001g0181 a0005c0025t0001g0187 |
2 | HG01109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1489-458A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 13/29 | chr3 | 129481072 | |||||||
| chr3:129481327 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1489-203G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 13/29 | chr3 | 129481327 | |||||||
| chr3:129481413 | T | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
100 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1489-117T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 13/29 | chr3 | 129481413 | |||||||
| chr3:129481929 | A | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
100 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1653+235A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129481929 | |||||||
| chr3:129481933 | C | T | 1 | a0002c0013t0001g0305 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1653+239C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129481933 | |||||||
| chr3:129481966 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1653+272C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129481966 | |||||||
| chr3:129481990 | G | A | 4 | a0002c0002t0001g0003 a0002c0002t0001g0299 a0002c0002t0001g0310 others(1): Show |
6 | HG01891.hp2 HG02451.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1653+296G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129481990 | |||||||
| chr3:129482125 | A | G | 1 | a0001c0001t0001g0281 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1653+431A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129482125 | |||||||
| chr3:129482251 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
171 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.1653+557C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129482251 | |||||||
| chr3:129482363 | C | T | 1 | a0002c0002t0001g0307 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1653+669C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129482363 | |||||||
| chr3:129482506 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0001g0116 |
4 | HG02258.hp2 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1653+812C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129482506 | |||||||
| chr3:129482520 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0076 |
2 | HG00558.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1653+826C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129482520 | |||||||
| chr3:129482529 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0136 a0001c0001t0001g0153 |
4 | HG00639.hp1 HG01981.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1653+835C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129482529 | |||||||
| chr3:129482642 | A | T | 1 | a0001c0001t0001g0229 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1654-843A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129482642 | |||||||
| chr3:129482839 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1654-646C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129482839 | |||||||
| chr3:129482849 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
171 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.1654-636A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129482849 | |||||||
| chr3:129482940 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(62): Show |
70 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1654-545G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129482940 | |||||||
| chr3:129483035 | G | C | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1654-450G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129483035 | |||||||
| chr3:129483185 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1654-300A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129483185 | |||||||
| chr3:129483257 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1654-228G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129483257 | |||||||
| chr3:129483258 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1654-227C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129483258 | |||||||
| chr3:129483282 | G | A | 1 | a0001c0004t0001g0322 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1654-203G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129483282 | |||||||
| chr3:129483306 | C | G | 2 | a0002c0002t0001g0317 a0002c0002t0001g0318 |
2 | HG00621.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1654-179C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129483306 | |||||||
| chr3:129483403 | A | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0002g0036 |
3 | HG01243.hp1 HG02486.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1654-82A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129483403 | |||||||
| chr3:129483473 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1654-12C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 14/29 | chr3 | 129483473 | |||||||
| chr3:129483801 | G | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
171 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.1851+119G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129483801 | |||||||
| chr3:129484010 | C | T | 6 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0303 others(3): Show |
8 | HG00544.hp2 HG02015.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.1851+328C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129484010 | |||||||
| chr3:129484018 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1851+336C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129484018 | |||||||
| chr3:129484032 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1851+350T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129484032 | |||||||
| chr3:129484155 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1851+473T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129484155 | |||||||
| chr3:129484172 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1851+490G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129484172 | |||||||
| chr3:129484431 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1851+749C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129484431 | |||||||
| chr3:129484440 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1851+758A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129484440 | |||||||
| chr3:129484659 | C | T | 27 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0002c0002t0001g0003 others(24): Show |
33 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.1851+977C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129484659 | |||||||
| chr3:129484778 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1851+1096T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129484778 | |||||||
| chr3:129484927 | T | A | 1 | a0001c0001t0001g0275 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1851+1245T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129484927 | |||||||
| chr3:129485113 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1851+1431T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129485113 | |||||||
| chr3:129485194 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
100 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1851+1512A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129485194 | |||||||
| chr3:129485210 | G | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG02622.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1851+1528G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129485210 | |||||||
| chr3:129485325 | G | C | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1851+1643G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129485325 | |||||||
| chr3:129485343 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1851+1661T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129485343 | |||||||
| chr3:129485484 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1851+1802G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129485484 | |||||||
| chr3:129485580 | C | T | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1851+1898C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129485580 | |||||||
| chr3:129485902 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1851+2220T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129485902 | |||||||
| chr3:129486101 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1852-2156A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129486101 | |||||||
| chr3:129486111 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1852-2146C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129486111 | |||||||
| chr3:129486223 | C | T | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1852-2034C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129486223 | |||||||
| chr3:129486237 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0215 |
3 | NA19066.hp2 NA19074.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1852-2020A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129486237 | |||||||
| chr3:129486542 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1852-1715A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129486542 | |||||||
| chr3:129486911 | C | T | 11 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(8): Show |
12 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.1852-1346C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129486911 | |||||||
| chr3:129487216 | A | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(20): Show |
25 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1852-1041A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487216 | |||||||
| chr3:129487302 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1852-955G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487302 | |||||||
| chr3:129487372 | TGCTG | T | 33 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(30): Show |
40 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.1852-883_1852-880d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr3 | 129487372 | ||||||
| chr3:129487376 | G | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1852-881G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487376 | |||||||
| chr3:129487416 | G | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
89 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1852-841G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487416 | |||||||
| chr3:129487455 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
235 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1852-802G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487455 | |||||||
| chr3:129487460 | G | T | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0003c0005t0001g0131 others(4): Show |
7 | HG02129.hp2 NA18957.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852-797G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487460 | |||||||
| chr3:129487514 | A | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG01109.hp1 HG03209.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1852-743A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487514 | |||||||
| chr3:129487551 | G | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0195 a0001c0001t0001g0281 others(16): Show |
21 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.1852-706G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487551 | |||||||
| chr3:129487594 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1852-663A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487594 | |||||||
| chr3:129487707 | C | T | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1852-550C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487707 | |||||||
| chr3:129487757 | C | CG | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(154): Show |
174 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.1852-498dupG | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr3 | 129487757 | ||||||
| chr3:129487778 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1852-479T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487778 | |||||||
| chr3:129487844 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0124 others(2): Show |
6 | HG00558.hp1 NA18942.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1852-413T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487844 | |||||||
| chr3:129487873 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0124 others(1): Show |
5 | HG02015.hp2 NA18960.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1852-384T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487873 | |||||||
| chr3:129487874 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0124 others(1): Show |
5 | HG02015.hp2 NA18960.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1852-383G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487874 | |||||||
| chr3:129487885 | G | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0124 |
4 | NA18960.hp2 NA18970.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1852-372G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487885 | |||||||
| chr3:129487937 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1852-320A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487937 | |||||||
| chr3:129487942 | C | G | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1852-315C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487942 | |||||||
| chr3:129487953 | G | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
210 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.1852-304G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487953 | |||||||
| chr3:129487955 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0032 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1852-302G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487955 | |||||||
| chr3:129487991 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0235 |
2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1852-266C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129487991 | |||||||
| chr3:129488004 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1852-253T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129488004 | |||||||
| chr3:129488042 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0228 |
2 | HG01928.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1852-215C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129488042 | |||||||
| chr3:129488056 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1852-201A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129488056 | |||||||
| chr3:129488082 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1852-175T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129488082 | |||||||
| chr3:129488125 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG03491.hp2 HG03492.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1852-132T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129488125 | |||||||
| chr3:129488128 | G | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG03491.hp2 HG03492.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1852-129G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 15/29 | chr3 | 129488128 | |||||||
| chr3:129488466 | C | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0045 others(54): Show |
66 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1992+69C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129488466 | |||||||
| chr3:129488524 | C | T | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1992+127C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129488524 | |||||||
| chr3:129488602 | A | G | 3 | a0001c0001t0001g0167 a0001c0001t0001g0293 a0002c0002t0001g0303 |
3 | HG00408.hp1 HG03471.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1992+205A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129488602 | |||||||
| chr3:129488631 | G | A | 1 | a0001c0015t0001g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1992+234G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129488631 | |||||||
| chr3:129488669 | C | T | 8 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(5): Show |
9 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1992+272C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129488669 | |||||||
| chr3:129488724 | A | T | 1 | a0001c0001t0001g0233 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1992+327A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129488724 | |||||||
| chr3:129488732 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(54): Show |
66 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1992+335A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129488732 | |||||||
| chr3:129488762 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1992+365G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129488762 | |||||||
| chr3:129488784 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1992+387G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129488784 | |||||||
| chr3:129488912 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1992+515C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129488912 | |||||||
| chr3:129489154 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1992+757C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489154 | |||||||
| chr3:129489317 | C | G | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1992+920C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489317 | |||||||
| chr3:129489469 | G | A | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG01496.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1992+1072G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489469 | |||||||
| chr3:129489564 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1992+1167C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489564 | |||||||
| chr3:129489615 | G | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1992+1218G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489615 | |||||||
| chr3:129489635 | C | T | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1992+1238C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489635 | |||||||
| chr3:129489754 | G | A | 5 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0303 others(2): Show |
7 | HG00544.hp2 HG02015.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1992+1357G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489754 | |||||||
| chr3:129489761 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1992+1364C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489761 | |||||||
| chr3:129489769 | GCGGAGCG others(19): Show |
G | 1 | a0001c0015t0001g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1992+1373_1992+139 others(30): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489769 | |||||||
| chr3:129489796 | G | T | 1 | a0001c0015t0001g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1992+1399G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489796 | |||||||
| chr3:129489797 | C | T | 1 | a0001c0015t0001g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1992+1400C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489797 | |||||||
| chr3:129489838 | T | TA | 69 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0045 others(66): Show |
76 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1992+1459dupA | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr3 | 129489838 | ||||||
| chr3:129489853 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1992+1456A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489853 | |||||||
| chr3:129489923 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1992+1526C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489923 | |||||||
| chr3:129489939 | C | T | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1992+1542C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129489939 | |||||||
| chr3:129490016 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1992+1619A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129490016 | |||||||
| chr3:129490113 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1992+1716T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129490113 | |||||||
| chr3:129490335 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
108 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1993-1806A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129490335 | |||||||
| chr3:129490628 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1993-1513A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129490628 | |||||||
| chr3:129490702 | C | G | 1 | a0001c0001t0001g0229 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1993-1439C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129490702 | |||||||
| chr3:129490747 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1993-1394G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129490747 | |||||||
| chr3:129491152 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1993-989G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491152 | |||||||
| chr3:129491299 | G | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1993-842G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491299 | |||||||
| chr3:129491480 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1993-661A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491480 | |||||||
| chr3:129491517 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1993-624C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491517 | |||||||
| chr3:129491553 | G | T | 1 | a0001c0001t0001g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1993-588G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491553 | |||||||
| chr3:129491616 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1993-525A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491616 | |||||||
| chr3:129491654 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0001g0116 |
4 | HG02258.hp2 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1993-487G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491654 | |||||||
| chr3:129491659 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1993-482A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491659 | |||||||
| chr3:129491701 | C | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG01109.hp1 HG03209.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1993-440C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491701 | |||||||
| chr3:129491795 | G | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1993-346G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491795 | |||||||
| chr3:129491817 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1993-324C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491817 | |||||||
| chr3:129491860 | G | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1993-281G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491860 | |||||||
| chr3:129491942 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0133 |
2 | HG00423.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1993-199A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129491942 | |||||||
| chr3:129492024 | C | A | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
65 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1993-117C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129492024 | |||||||
| chr3:129492133 | C | T | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | splice_region_variant&intron_variant | LOW | c.1993-8C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129492133 | |||||||
| chr3:129492134 | G | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(231): Show |
256 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(253): Show |
splice_region_variant&intron_variant | LOW | c.1993-7G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 16/29 | chr3 | 129492134 | |||||||
| chr3:129492218 | T | C | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2046+24T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129492218 | |||||||
| chr3:129492226 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.2046+32A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129492226 | |||||||
| chr3:129492334 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2046+140C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129492334 | |||||||
| chr3:129492337 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0236 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2046+143C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129492337 | |||||||
| chr3:129492502 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2046+308C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129492502 | |||||||
| chr3:129492532 | C | T | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2046+338C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129492532 | |||||||
| chr3:129492563 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2046+369A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129492563 | |||||||
| chr3:129492584 | G | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2046+390G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129492584 | |||||||
| chr3:129492804 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2046+610T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129492804 | |||||||
| chr3:129492805 | GCTTTTTT others(3): Show |
G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0063 |
3 | NA18995.hp1 NA19057.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.2046+622_2046+631d others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr3 | 129492805 | ||||||
| chr3:129492816 | C | CT | 43 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(40): Show |
47 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.2046+640dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr3 | 129492816 | ||||||
| chr3:129492816 | C | CTT | 20 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0118 others(17): Show |
20 | HG00423.hp1 HG00621.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2046+639_2046+640d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr3 | 129492816 | ||||||
| chr3:129492816 | CT | C | 6 | a0001c0001t0001g0204 a0001c0001t0001g0216 a0001c0001t0001g0239 others(3): Show |
6 | HG00735.hp1 HG03471.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.2046+640delT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr3 | 129492816 | ||||||
| chr3:129492822 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2046+628T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129492822 | |||||||
| chr3:129492870 | G | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0283 others(14): Show |
19 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.2046+676G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129492870 | |||||||
| chr3:129493018 | A | G | 13 | a0001c0001t0001g0012 a0001c0001t0001g0121 a0001c0001t0001g0123 others(10): Show |
14 | HG01069.hp2 HG01071.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.2046+824A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129493018 | |||||||
| chr3:129493039 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2046+845A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129493039 | |||||||
| chr3:129493044 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2046+850G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129493044 | |||||||
| chr3:129493156 | G | A | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.2046+962G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129493156 | |||||||
| chr3:129493334 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2046+1140C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129493334 | |||||||
| chr3:129493428 | G | A | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
65 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.2046+1234G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129493428 | |||||||
| chr3:129493508 | A | G | 1 | a0003c0005t0001g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2046+1314A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129493508 | |||||||
| chr3:129493557 | C | T | 1 | a0002c0002t0001g0317 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2046+1363C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129493557 | |||||||
| chr3:129493582 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2046+1388C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129493582 | |||||||
| chr3:129493974 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2047-1472A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129493974 | |||||||
| chr3:129493981 | T | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2047-1465T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129493981 | |||||||
| chr3:129494074 | C | T | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
65 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.2047-1372C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129494074 | |||||||
| chr3:129494095 | T | C | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2047-1351T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129494095 | |||||||
| chr3:129494126 | C | T | 6 | a0002c0002t0001g0301 a0002c0002t0001g0309 a0002c0002t0001g0313 others(3): Show |
6 | HG00408.hp2 HG00621.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.2047-1320C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129494126 | |||||||
| chr3:129494212 | G | GT | 19 | a0001c0001t0001g0002 a0001c0001t0001g0282 a0001c0001t0001g0283 others(16): Show |
21 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.2047-1231dupT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr3 | 129494212 | ||||||
| chr3:129494214 | T | TG | 34 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(31): Show |
41 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2047-1232_2047-123 others(5): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129494214 | |||||||
| chr3:129494216 | G | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2047-1230G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129494216 | |||||||
| chr3:129494220 | T | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
93 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.2047-1226T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129494220 | |||||||
| chr3:129494428 | G | A | 1 | a0002c0002t0001g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2047-1018G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129494428 | |||||||
| chr3:129494532 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2047-914G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129494532 | |||||||
| chr3:129494628 | G | A | 3 | a0004c0006t0001g0285 a0004c0006t0001g0286 a0004c0006t0001g0324 |
3 | HG02083.hp1 HG03834.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.2047-818G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129494628 | |||||||
| chr3:129494682 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2047-764C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129494682 | |||||||
| chr3:129494685 | A | AGT | 4 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0009t0001g0099 others(1): Show |
4 | HG00735.hp1 HG02280.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2047-738_2047-737d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr3 | 129494685 | ||||||
| chr3:129494685 | A | AGTGT | 34 | a0001c0001t0001g0282 a0001c0004t0001g0021 a0001c0004t0001g0322 others(31): Show |
41 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.2047-740_2047-737d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr3 | 129494685 | ||||||
| chr3:129494685 | A | AGTGTGT | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(80): Show |
90 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.2047-742_2047-737d others(8): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr3 | 129494685 | ||||||
| chr3:129494685 | AGT | A | 145 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(142): Show |
152 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2047-738_2047-737d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr3 | 129494685 | ||||||
| chr3:129494725 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2047-721T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129494725 | |||||||
| chr3:129494782 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0236 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2047-664C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129494782 | |||||||
| chr3:129495062 | C | T | 1 | a0001c0024t0001g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2047-384C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129495062 | |||||||
| chr3:129495273 | G | A | 1 | a0002c0002t0001g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2047-173G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 17/29 | chr3 | 129495273 | |||||||
| chr3:129495668 | G | A | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.2208+61G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129495668 | |||||||
| chr3:129495737 | G | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
100 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.2208+130G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129495737 | |||||||
| chr3:129495770 | C | T | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2208+163C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129495770 | |||||||
| chr3:129495782 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2208+175C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129495782 | |||||||
| chr3:129495814 | G | A | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
65 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.2208+207G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129495814 | |||||||
| chr3:129495846 | A | G | 12 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
12 | HG00544.hp1 HG02132.hp2 HG03490.hp2 others(9): Show |
intron_variant | MODIFIER | c.2208+239A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129495846 | |||||||
| chr3:129495882 | A | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0245 |
2 | HG02293.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.2208+275A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129495882 | |||||||
| chr3:129495926 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
170 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.2208+319C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129495926 | |||||||
| chr3:129496011 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2208+404G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129496011 | |||||||
| chr3:129496202 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
129 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.2208+595C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129496202 | |||||||
| chr3:129496304 | G | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0190 |
2 | NA18951.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.2208+697G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129496304 | |||||||
| chr3:129496372 | C | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2208+765C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129496372 | |||||||
| chr3:129496609 | T | G | 1 | a0001c0001t0001g0067 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2208+1002T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129496609 | |||||||
| chr3:129496816 | G | A | 1 | a0009c0021t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2208+1209G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129496816 | |||||||
| chr3:129496825 | A | C | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.2208+1218A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129496825 | |||||||
| chr3:129496874 | A | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | NA18995.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2208+1267A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129496874 | |||||||
| chr3:129496930 | A | T | 1 | a0001c0001t0001g0067 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2208+1323A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129496930 | |||||||
| chr3:129497094 | A | G | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2208+1487A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497094 | |||||||
| chr3:129497107 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2208+1500C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497107 | |||||||
| chr3:129497132 | A | G | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2208+1525A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497132 | |||||||
| chr3:129497196 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2208+1589A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497196 | |||||||
| chr3:129497224 | C | T | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2208+1617C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497224 | |||||||
| chr3:129497279 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2208+1672T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497279 | |||||||
| chr3:129497279 | T | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(223): Show |
247 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.2208+1672T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497279 | |||||||
| chr3:129497290 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(17): Show |
22 | HG00735.hp1 HG01255.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.2208+1683G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497290 | |||||||
| chr3:129497296 | G | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | NA18952.hp2 NA18956.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2208+1689G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497296 | |||||||
| chr3:129497332 | T | G | 1 | a0001c0001t0001g0067 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2208+1725T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497332 | |||||||
| chr3:129497333 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2208+1726G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497333 | |||||||
| chr3:129497354 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2208+1747C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497354 | |||||||
| chr3:129497358 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2208+1751G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497358 | |||||||
| chr3:129497448 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2208+1841G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497448 | |||||||
| chr3:129497529 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2208+1922C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497529 | |||||||
| chr3:129497647 | C | A | 1 | a0001c0016t0001g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2208+2040C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497647 | |||||||
| chr3:129497741 | G | A | 6 | a0001c0004t0001g0021 a0001c0004t0001g0326 a0001c0004t0001g0327 others(3): Show |
7 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.2208+2134G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497741 | |||||||
| chr3:129497820 | AC | A | 25 | a0002c0002t0001g0003 a0002c0002t0001g0017 a0002c0002t0001g0018 others(22): Show |
31 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.2209-2081delC | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497820 | |||||||
| chr3:129497829 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(223): Show |
247 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.2209-2073A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497829 | |||||||
| chr3:129497846 | A | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
69 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2209-2056A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497846 | |||||||
| chr3:129497925 | T | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2209-1977T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129497925 | |||||||
| chr3:129498049 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0030 |
3 | HG00738.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2209-1853A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498049 | |||||||
| chr3:129498174 | C | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2209-1728C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498174 | |||||||
| chr3:129498327 | GT | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0235 |
3 | HG01070.hp2 HG01074.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2209-1571delT | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr3 | 129498327 | ||||||
| chr3:129498340 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2209-1562T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498340 | |||||||
| chr3:129498348 | T | G | 29 | a0001c0001t0001g0011 a0001c0001t0001g0117 a0001c0001t0001g0118 others(26): Show |
30 | HG00423.hp1 HG00621.hp1 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.2209-1554T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498348 | |||||||
| chr3:129498405 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2209-1497C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498405 | |||||||
| chr3:129498458 | G | A | 1 | a0012c0017t0001g0114 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2209-1444G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498458 | |||||||
| chr3:129498484 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0283 others(14): Show |
19 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.2209-1418C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498484 | |||||||
| chr3:129498490 | T | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2209-1412T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498490 | |||||||
| chr3:129498608 | G | A | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2209-1294G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498608 | |||||||
| chr3:129498635 | C | T | 37 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0320 others(34): Show |
44 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.2209-1267C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498635 | |||||||
| chr3:129498703 | C | G | 50 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(47): Show |
54 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.2209-1199C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498703 | |||||||
| chr3:129498716 | T | C | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2209-1186T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498716 | |||||||
| chr3:129498844 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2209-1058G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498844 | |||||||
| chr3:129498895 | T | C | 4 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0108 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2209-1007T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498895 | |||||||
| chr3:129498931 | A | T | 1 | a0001c0001t0001g0243 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2209-971A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498931 | |||||||
| chr3:129498970 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2209-932C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129498970 | |||||||
| chr3:129499054 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
97 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.2209-848T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129499054 | |||||||
| chr3:129499125 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0123 a0001c0001t0001g0173 others(54): Show |
66 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.2209-777T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129499125 | |||||||
| chr3:129499154 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0076 |
2 | HG00558.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.2209-748C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129499154 | |||||||
| chr3:129499206 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2209-696A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129499206 | |||||||
| chr3:129499213 | T | C | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2209-689T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129499213 | |||||||
| chr3:129499313 | G | A | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2209-589G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129499313 | |||||||
| chr3:129499348 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2209-554G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129499348 | |||||||
| chr3:129499420 | AAGC | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
169 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.2209-480_2209-478d others(5): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr3 | 129499420 | ||||||
| chr3:129499466 | G | T | 1 | a0001c0001t0001g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2209-436G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129499466 | |||||||
| chr3:129499605 | G | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2209-297G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129499605 | |||||||
| chr3:129499791 | G | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | NA19003.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2209-111G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129499791 | |||||||
| chr3:129499837 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2209-65G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 18/29 | chr3 | 129499837 | |||||||
| chr3:129500101 | G | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2375+33G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129500101 | |||||||
| chr3:129500132 | T | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2375+64T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129500132 | |||||||
| chr3:129500293 | C | T | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2375+225C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129500293 | |||||||
| chr3:129500521 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2375+453C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129500521 | |||||||
| chr3:129500667 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
20 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.2375+599C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129500667 | |||||||
| chr3:129500806 | C | T | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2375+738C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129500806 | |||||||
| chr3:129500877 | G | T | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2375+809G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129500877 | |||||||
| chr3:129500926 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2375+858G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129500926 | |||||||
| chr3:129500986 | A | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG01109.hp1 HG03209.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2375+918A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129500986 | |||||||
| chr3:129501082 | G | A | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.2375+1014G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501082 | |||||||
| chr3:129501131 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
20 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.2375+1063G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501131 | |||||||
| chr3:129501135 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2375+1067C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501135 | |||||||
| chr3:129501144 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
235 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.2375+1076G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501144 | |||||||
| chr3:129501153 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
72 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.2375+1085G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501153 | |||||||
| chr3:129501169 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2375+1101C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501169 | |||||||
| chr3:129501211 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2375+1143C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501211 | |||||||
| chr3:129501508 | A | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | NA18957.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2376-1203A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501508 | |||||||
| chr3:129501642 | C | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2376-1069C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501642 | |||||||
| chr3:129501695 | T | C | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2376-1016T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501695 | |||||||
| chr3:129501705 | G | T | 32 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0117 others(29): Show |
34 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.2376-1006G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501705 | |||||||
| chr3:129501840 | C | T | 2 | a0001c0001t0001g0261 a0001c0020t0001g0260 |
2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2376-871C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501840 | |||||||
| chr3:129501953 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2376-758C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501953 | |||||||
| chr3:129501953 | C | T | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2376-758C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501953 | |||||||
| chr3:129501967 | G | T | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2376-744G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501967 | |||||||
| chr3:129501979 | C | G | 1 | a0001c0015t0001g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2376-732C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129501979 | |||||||
| chr3:129502006 | A | C | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2376-705A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129502006 | |||||||
| chr3:129502048 | G | A | 33 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(30): Show |
40 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.2376-663G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129502048 | |||||||
| chr3:129502139 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2376-572G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129502139 | |||||||
| chr3:129502248 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2376-463G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129502248 | |||||||
| chr3:129502464 | G | C | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2376-247G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129502464 | |||||||
| chr3:129502506 | C | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
20 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.2376-205C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 19/29 | chr3 | 129502506 | |||||||
| chr3:129503349 | TC | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0102 others(7): Show |
11 | HG01109.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2547+470delC | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr3 | 129503349 | ||||||
| chr3:129503364 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(31): Show |
39 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.2547+482C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 20/29 | chr3 | 129503364 | |||||||
| chr3:129503372 | A | T | 1 | a0001c0001t0001g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2547+490A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 20/29 | chr3 | 129503372 | |||||||
| chr3:129503446 | C | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
90 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.2547+564C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 20/29 | chr3 | 129503446 | |||||||
| chr3:129503610 | A | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2548-709A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 20/29 | chr3 | 129503610 | |||||||
| chr3:129503706 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0201 |
2 | HG00642.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2548-613G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 20/29 | chr3 | 129503706 | |||||||
| chr3:129503885 | C | T | 10 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(7): Show |
10 | HG02132.hp2 HG03490.hp2 HG03492.hp2 others(7): Show |
intron_variant | MODIFIER | c.2548-434C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 20/29 | chr3 | 129503885 | |||||||
| chr3:129504134 | T | C | 2 | a0001c0001t0001g0035 a0006c0010t0001g0193 |
2 | HG01175.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.2548-185T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 20/29 | chr3 | 129504134 | |||||||
| chr3:129504268 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2548-51T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 20/29 | chr3 | 129504268 | |||||||
| chr3:129504699 | C | G | 1 | a0001c0020t0001g0260 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2650+278C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129504699 | |||||||
| chr3:129504715 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG01109.hp1 HG03209.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2650+294C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129504715 | |||||||
| chr3:129504736 | C | G | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2650+315C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129504736 | |||||||
| chr3:129504823 | CAT | C | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2650+404_2650+405d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr3 | 129504823 | ||||||
| chr3:129504865 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2650+444C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129504865 | |||||||
| chr3:129504909 | T | TCTCAC | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): Show |
163 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.2650+491_2650+492i others(7): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr3 | 129504909 | ||||||
| chr3:129505072 | T | C | 1 | a0002c0002t0001g0307 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2650+651T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129505072 | |||||||
| chr3:129505079 | T | A | 1 | a0001c0001t0001g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2650+658T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129505079 | |||||||
| chr3:129505106 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2650+685G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129505106 | |||||||
| chr3:129505159 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2650+738A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129505159 | |||||||
| chr3:129505263 | T | G | 37 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0320 others(34): Show |
44 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.2650+842T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129505263 | |||||||
| chr3:129505288 | G | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
236 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.2650+867G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129505288 | |||||||
| chr3:129505350 | C | T | 37 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0320 others(34): Show |
44 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.2650+929C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129505350 | |||||||
| chr3:129505394 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2650+973C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129505394 | |||||||
| chr3:129505682 | C | A | 1 | a0001c0020t0001g0260 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2651-727C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129505682 | |||||||
| chr3:129505754 | G | A | 8 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
8 | HG03490.hp2 HG03492.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.2651-655G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129505754 | |||||||
| chr3:129506032 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2651-377G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129506032 | |||||||
| chr3:129506138 | A | G | 2 | a0002c0002t0001g0317 a0002c0002t0001g0318 |
2 | HG00621.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2651-271A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129506138 | |||||||
| chr3:129506215 | C | G | 1 | a0002c0002t0001g0017 | 2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.2651-194C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129506215 | |||||||
| chr3:129506293 | C | T | 1 | a0003c0005t0001g0152 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2651-116C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 21/29 | chr3 | 129506293 | |||||||
| chr3:129506575 | G | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG01496.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2791+26G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 22/29 | chr3 | 129506575 | |||||||
| chr3:129506654 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2791+105A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 22/29 | chr3 | 129506654 | |||||||
| chr3:129506691 | G | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2791+142G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 22/29 | chr3 | 129506691 | |||||||
| chr3:129506823 | A | G | 6 | a0001c0004t0001g0021 a0001c0004t0001g0326 a0001c0004t0001g0327 others(3): Show |
7 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.2791+274A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 22/29 | chr3 | 129506823 | |||||||
| chr3:129507124 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
69 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2792-544C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 22/29 | chr3 | 129507124 | |||||||
| chr3:129507150 | C | G | 1 | a0001c0001t0001g0124 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2792-518C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 22/29 | chr3 | 129507150 | |||||||
| chr3:129507239 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2792-429T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 22/29 | chr3 | 129507239 | |||||||
| chr3:129507253 | A | G | 62 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
66 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.2792-415A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 22/29 | chr3 | 129507253 | |||||||
| chr3:129507818 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2886+56C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129507818 | |||||||
| chr3:129507818 | C | T | 1 | a0001c0022t0001g0251 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2886+56C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129507818 | |||||||
| chr3:129507912 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2886+150T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129507912 | |||||||
| chr3:129508355 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2886+593A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129508355 | |||||||
| chr3:129508395 | A | G | 29 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0162 others(26): Show |
30 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2886+633A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129508395 | |||||||
| chr3:129508466 | C | T | 61 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(58): Show |
65 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.2886+704C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129508466 | |||||||
| chr3:129508763 | G | A | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2886+1001G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129508763 | |||||||
| chr3:129508808 | C | CG | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
235 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.2886+1047dupG | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr3 | 129508808 | ||||||
| chr3:129509289 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2886+1527C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129509289 | |||||||
| chr3:129509323 | TCTC | T | 35 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(32): Show |
42 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.2886+1564_2886+156 others(7): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr3 | 129509323 | ||||||
| chr3:129509479 | G | T | 1 | a0001c0001t0001g0293 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2886+1717G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129509479 | |||||||
| chr3:129509488 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2886+1726C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129509488 | |||||||
| chr3:129509551 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2886+1789C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129509551 | |||||||
| chr3:129509665 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2886+1903A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129509665 | |||||||
| chr3:129509908 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2886+2146C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129509908 | |||||||
| chr3:129509973 | A | G | 1 | a0001c0001t0001g0281 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2886+2211A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129509973 | |||||||
| chr3:129510140 | A | C | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG01496.hp1 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2887-2172A>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129510140 | |||||||
| chr3:129510142 | C | T | 1 | a0001c0001t0001g0320 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2887-2170C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129510142 | |||||||
| chr3:129510217 | C | T | 1 | a0001c0016t0001g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2887-2095C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129510217 | |||||||
| chr3:129510749 | C | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0266 |
3 | HG02970.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2887-1563C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129510749 | |||||||
| chr3:129511489 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2887-823G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129511489 | |||||||
| chr3:129511723 | G | A | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2887-589G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129511723 | |||||||
| chr3:129511761 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
12 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2887-551C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129511761 | |||||||
| chr3:129512083 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2887-229G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129512083 | |||||||
| chr3:129512094 | C | CAGT | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0266 |
3 | HG02970.hp1 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2887-216_2887-214d others(5): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr3 | 129512094 | ||||||
| chr3:129512161 | A | T | 1 | a0009c0021t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2887-151A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129512161 | |||||||
| chr3:129512167 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2887-145C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 23/29 | chr3 | 129512167 | |||||||
| chr3:129512565 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2987+153T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129512565 | |||||||
| chr3:129512590 | G | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
91 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.2987+178G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129512590 | |||||||
| chr3:129512704 | T | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2987+292T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129512704 | |||||||
| chr3:129512733 | C | T | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2987+321C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129512733 | |||||||
| chr3:129512845 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2987+433C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129512845 | |||||||
| chr3:129512860 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02071.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2987+448G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129512860 | |||||||
| chr3:129513008 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | NA18943.hp2 NA19076.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2987+596G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513008 | |||||||
| chr3:129513121 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0116 |
3 | HG02258.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2987+709G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513121 | |||||||
| chr3:129513156 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0199 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2987+744C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513156 | |||||||
| chr3:129513157 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2987+745G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513157 | |||||||
| chr3:129513213 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2987+801A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513213 | |||||||
| chr3:129513290 | T | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2987+878T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513290 | |||||||
| chr3:129513495 | C | T | 6 | a0001c0004t0001g0021 a0001c0004t0001g0326 a0001c0004t0001g0327 others(3): Show |
7 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.2988-894C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513495 | |||||||
| chr3:129513511 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
91 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.2988-878C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513511 | |||||||
| chr3:129513552 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2988-837T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513552 | |||||||
| chr3:129513803 | A | G | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2988-586A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513803 | |||||||
| chr3:129513808 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2988-581A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513808 | |||||||
| chr3:129513844 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG02735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2988-545C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513844 | |||||||
| chr3:129513845 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
20 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.2988-544G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513845 | |||||||
| chr3:129513886 | C | CAGGCG | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
236 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.2988-499_2988-498i others(7): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr3 | 129513886 | ||||||
| chr3:129513921 | G | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
20 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.2988-468G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513921 | |||||||
| chr3:129513929 | G | C | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2988-460G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513929 | |||||||
| chr3:129513999 | G | C | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2988-390G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129513999 | |||||||
| chr3:129514177 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2988-212G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129514177 | |||||||
| chr3:129514244 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
69 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2988-145G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129514244 | |||||||
| chr3:129514244 | G | T | 8 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(5): Show |
9 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.2988-145G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129514244 | |||||||
| chr3:129514298 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2988-91G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129514298 | |||||||
| chr3:129514330 | G | C | 1 | a0001c0001t0001g0261 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2988-59G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 24/29 | chr3 | 129514330 | |||||||
| chr3:129514676 | C | A | 1 | a0001c0001t0001g0059 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3153+122C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129514676 | |||||||
| chr3:129514709 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3153+155T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129514709 | |||||||
| chr3:129514770 | C | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(13): Show |
17 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.3153+216C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129514770 | |||||||
| chr3:129514915 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.3153+361C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129514915 | |||||||
| chr3:129514918 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3153+364G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129514918 | |||||||
| chr3:129514993 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0199 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3153+439C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129514993 | |||||||
| chr3:129515003 | T | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3153+449T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129515003 | |||||||
| chr3:129515130 | G | A | 1 | a0001c0024t0001g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3154-358G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129515130 | |||||||
| chr3:129515164 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.3154-324G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129515164 | |||||||
| chr3:129515209 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3154-279G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129515209 | |||||||
| chr3:129515412 | G | A | 1 | a0002c0002t0001g0302 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3154-76G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129515412 | |||||||
| chr3:129515416 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
236 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.3154-72T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129515416 | |||||||
| chr3:129515446 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3154-42G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 25/29 | chr3 | 129515446 | |||||||
| chr3:129515606 | C | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.3265+7C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129515606 | |||||||
| chr3:129515658 | C | G | 1 | a0002c0002t0001g0017 | 2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.3265+59C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129515658 | |||||||
| chr3:129515681 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0001g0116 |
4 | HG02258.hp2 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3265+82G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129515681 | |||||||
| chr3:129515819 | C | G | 1 | a0004c0006t0001g0286 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3265+220C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129515819 | |||||||
| chr3:129515863 | A | G | 6 | a0001c0003t0001g0269 a0001c0003t0001g0270 a0001c0003t0001g0271 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3265+264A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129515863 | |||||||
| chr3:129516063 | C | T | 1 | a0001c0016t0001g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3265+464C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516063 | |||||||
| chr3:129516098 | GCA | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
169 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.3265+512_3265+513d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516098 | ||||||
| chr3:129516119 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3265+520C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516119 | |||||||
| chr3:129516157 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3265+558G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516157 | |||||||
| chr3:129516169 | GCA | G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
12 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.3265+583_3265+584d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516169 | ||||||
| chr3:129516219 | GCACA | G | 33 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(30): Show |
40 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.3265+629_3265+632d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516219 | ||||||
| chr3:129516223 | ACACACAC others(16): Show |
A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0076 |
2 | HG00558.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.3265+643_3265+665d others(25): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516223 | ||||||
| chr3:129516286 | G | GCA | 5 | a0001c0001t0001g0051 a0001c0001t0001g0232 a0001c0001t0001g0245 others(2): Show |
5 | HG00735.hp1 HG02293.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.3265+708_3265+709d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516286 | ||||||
| chr3:129516286 | G | GCACACAC others(1): Show |
4 | a0001c0003t0001g0269 a0001c0003t0001g0271 a0001c0003t0001g0273 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.3265+702_3265+709d others(10): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516286 | ||||||
| chr3:129516286 | G | GCACACAC others(3): Show |
1 | a0001c0003t0001g0270 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3265+700_3265+709d others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516286 | ||||||
| chr3:129516286 | GCACA | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0022 others(19): Show |
24 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.3265+706_3265+709d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516286 | ||||||
| chr3:129516298 | ACACACAC others(16): Show |
A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0284 others(13): Show |
18 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.3265+733_3265+755d others(25): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516298 | ||||||
| chr3:129516302 | ACACACAG others(12): Show |
A | 1 | a0001c0001t0001g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3265+710_3265+728d others(21): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516302 | ||||||
| chr3:129516307 | C | G | 1 | a0009c0021t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3265+708C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516307 | |||||||
| chr3:129516307 | CAG | C | 60 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(57): Show |
64 | HG00423.hp1 HG00621.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.3265+712_3265+713d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516307 | ||||||
| chr3:129516460 | CGCCCCTG others(18): Show |
C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
20 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.3265+895_3265+919d others(27): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516460 | ||||||
| chr3:129516478 | T | G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3265+879T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516478 | |||||||
| chr3:129516538 | CCCTGCAC others(14): Show |
C | 1 | a0002c0002t0001g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3266-916_3266-896d others(23): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516538 | ||||||
| chr3:129516544 | ACACACAC others(12): Show |
A | 27 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(24): Show |
32 | HG00140.hp1 HG00408.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.3266-916_3266-898d others(21): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516544 | ||||||
| chr3:129516551 | C | CACACACA others(534): Show |
5 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0303 others(2): Show |
7 | HG00544.hp2 HG02015.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.3266-917_3266-916i others(543): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516551 | ||||||
| chr3:129516555 | T | C | 5 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0303 others(2): Show |
7 | HG00544.hp2 HG02015.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.3266-914T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516555 | |||||||
| chr3:129516559 | T | C | 5 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0303 others(2): Show |
7 | HG00544.hp2 HG02015.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.3266-910T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516559 | |||||||
| chr3:129516563 | G | GCA | 6 | a0001c0001t0001g0281 a0002c0002t0001g0017 a0002c0002t0001g0018 others(3): Show |
8 | HG00544.hp2 HG02015.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.3266-891_3266-890d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516563 | ||||||
| chr3:129516563 | GCA | G | 3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0233 |
3 | HG02602.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3266-891_3266-890d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516563 | ||||||
| chr3:129516578 | CAG | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0262 |
3 | HG02976.hp2 NA18995.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3266-885_3266-884d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516578 | ||||||
| chr3:129516580 | G | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(207): Show |
230 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.3266-889G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516580 | |||||||
| chr3:129516582 | G | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0325 a0001c0016t0001g0149 |
3 | HG02886.hp1 NA18612.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.3266-887G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516582 | |||||||
| chr3:129516605 | G | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
88 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.3266-864G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516605 | |||||||
| chr3:129516693 | T | TGC | 3 | a0001c0001t0001g0002 a0001c0001t0001g0287 a0001c0001t0001g0288 |
5 | HG01255.hp1 HG02055.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3266-775_3266-774d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516693 | ||||||
| chr3:129516694 | G | GCA | 27 | a0001c0001t0001g0016 a0001c0001t0001g0113 a0001c0001t0001g0153 others(24): Show |
29 | HG00140.hp1 HG00609.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.3266-744_3266-743d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516694 | ||||||
| chr3:129516694 | G | GCACA | 3 | a0001c0004t0001g0322 a0001c0012t0001g0268 a0001c0022t0001g0251 |
3 | HG02257.hp1 HG02976.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.3266-746_3266-743d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516694 | ||||||
| chr3:129516694 | G | GCGCACAC others(3): Show |
2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3266-774_3266-773i others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516694 | ||||||
| chr3:129516694 | G | GCGCGCAC others(3): Show |
1 | a0001c0001t0001g0298 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3266-774_3266-773i others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516694 | ||||||
| chr3:129516694 | G | GCGCGCAC others(5): Show |
1 | a0001c0001t0001g0296 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3266-774_3266-773i others(14): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516694 | ||||||
| chr3:129516694 | G | GCGCGCGC others(3): Show |
1 | a0004c0006t0001g0286 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3266-774_3266-773i others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516694 | ||||||
| chr3:129516694 | GCA | G | 34 | a0001c0001t0001g0012 a0001c0001t0001g0120 a0001c0001t0001g0121 others(31): Show |
35 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.3266-744_3266-743d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516694 | ||||||
| chr3:129516694 | GCACACA | G | 4 | a0001c0001t0001g0159 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | HG02735.hp1 HG03239.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.3266-748_3266-743d others(8): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516694 | ||||||
| chr3:129516694 | GCACACAC others(1): Show |
G | 11 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(8): Show |
12 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.3266-750_3266-743d others(10): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516694 | ||||||
| chr3:129516694 | GCACACAC others(3): Show |
G | 5 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0104 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3266-752_3266-743d others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516694 | ||||||
| chr3:129516713 | CACACACA others(7): Show |
C | 2 | a0002c0002t0001g0018 a0002c0002t0001g0307 |
3 | HG02015.hp1 NA18999.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3266-754_3266-741d others(16): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516713 | ||||||
| chr3:129516715 | C | G | 1 | a0002c0002t0001g0306 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3266-754C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516715 | |||||||
| chr3:129516715 | CACACACA others(5): Show |
C | 21 | a0002c0002t0001g0003 a0002c0002t0001g0017 a0002c0002t0001g0019 others(18): Show |
26 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3266-752_3266-741d others(14): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516715 | ||||||
| chr3:129516716 | A | AGACTGCC others(4): Show |
1 | a0002c0002t0001g0306 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3266-753_3266-752i others(13): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516716 | |||||||
| chr3:129516717 | CACACACA others(3): Show |
C | 1 | a0002c0002t0001g0299 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3266-750_3266-741d others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516717 | ||||||
| chr3:129516721 | CACACAG | C | 8 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0052 others(5): Show |
8 | HG00621.hp1 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.3266-746_3266-741d others(8): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516721 | ||||||
| chr3:129516723 | C | G | 1 | a0001c0001t0001g0230 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3266-746C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516723 | |||||||
| chr3:129516723 | CACAG | C | 9 | a0001c0001t0001g0051 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.3266-744_3266-741d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516723 | ||||||
| chr3:129516725 | C | G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0194 a0001c0001t0001g0230 |
3 | HG00735.hp2 HG01167.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3266-744C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516725 | |||||||
| chr3:129516725 | CAG | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
85 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.3266-738_3266-737d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516725 | ||||||
| chr3:129516727 | G | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(77): Show |
86 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.3266-742G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516727 | |||||||
| chr3:129516729 | G | C | 2 | a0001c0001t0001g0222 a0002c0002t0001g0306 |
2 | NA18950.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.3266-740G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516729 | |||||||
| chr3:129516729 | G | GAGACTGC others(18): Show |
1 | a0001c0001t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3266-721_3266-697d others(27): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516729 | ||||||
| chr3:129516793 | GCACACAC others(18): Show |
G | 1 | a0001c0001t0001g0156 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3266-640_3266-616d others(27): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516793 | ||||||
| chr3:129516804 | G | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0283 others(51): Show |
63 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.3266-665G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516804 | |||||||
| chr3:129516816 | GCACACAC others(20): Show |
G | 1 | a0001c0001t0001g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3266-640_3266-614d others(29): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516816 | ||||||
| chr3:129516827 | CAG | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG01255.hp2 HG01975.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.3266-638_3266-637d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129516827 | ||||||
| chr3:129516829 | G | C | 21 | a0001c0001t0001g0015 a0001c0001t0001g0049 a0001c0001t0001g0063 others(18): Show |
22 | HG00597.hp2 HG00609.hp2 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.3266-640G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516829 | |||||||
| chr3:129516847 | A | G | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3266-622A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516847 | |||||||
| chr3:129516858 | G | C | 37 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0320 others(34): Show |
44 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.3266-611G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516858 | |||||||
| chr3:129516861 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(52): Show |
64 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.3266-608G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516861 | |||||||
| chr3:129516911 | C | T | 3 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0012t0001g0268 |
3 | HG01243.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3266-558C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129516911 | |||||||
| chr3:129517006 | G | C | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3266-463G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129517006 | |||||||
| chr3:129517039 | GCA | G | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | NA18952.hp2 NA18956.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3266-409_3266-408d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517039 | ||||||
| chr3:129517060 | C | CACACAG | 4 | a0002c0002t0001g0018 a0002c0002t0001g0303 a0002c0002t0001g0306 others(1): Show |
5 | HG02015.hp1 HG04228.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.3266-408_3266-407i others(8): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517060 | ||||||
| chr3:129517060 | C | CAG | 29 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0004t0001g0021 others(26): Show |
34 | HG00140.hp1 HG00408.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.3266-407_3266-406d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517060 | ||||||
| chr3:129517060 | C | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(188): Show |
206 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.3266-409C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129517060 | |||||||
| chr3:129517085 | G | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3266-384G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129517085 | |||||||
| chr3:129517121 | C | CCTGCACA others(41): Show |
2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3266-334_3266-287d others(50): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517121 | ||||||
| chr3:129517135 | T | TGGAGACT others(16): Show |
1 | a0001c0007t0001g0328 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3266-323_3266-301d others(25): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517135 | ||||||
| chr3:129517146 | CCTGCACA others(16): Show |
C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG01884.hp1 HG02809.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3266-310_3266-288d others(25): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517146 | ||||||
| chr3:129517183 | G | C | 1 | a0001c0007t0001g0328 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3266-286G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129517183 | |||||||
| chr3:129517194 | TACAC | T | 8 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(5): Show |
8 | HG02559.hp1 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3266-265_3266-262d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517194 | ||||||
| chr3:129517218 | G | GCA | 7 | a0001c0001t0001g0207 a0001c0003t0001g0269 a0001c0003t0001g0270 others(4): Show |
7 | HG01074.hp2 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.3266-236_3266-235d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517218 | ||||||
| chr3:129517243 | C | G | 3 | a0002c0002t0001g0018 a0002c0002t0001g0306 a0002c0002t0001g0307 |
4 | HG02015.hp1 NA18950.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.3266-226C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129517243 | |||||||
| chr3:129517268 | G | GCA | 79 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
82 | HG00423.hp1 HG00423.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.3266-168_3266-167d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517268 | ||||||
| chr3:129517268 | G | GCACA | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(58): Show |
66 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.3266-170_3266-167d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517268 | ||||||
| chr3:129517268 | G | GCACACA | 16 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0037 others(13): Show |
17 | HG00544.hp1 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.3266-172_3266-167d others(8): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517268 | ||||||
| chr3:129517268 | G | GCACACAC others(1): Show |
3 | a0001c0001t0001g0056 a0001c0001t0001g0111 a0001c0001t0001g0148 |
3 | HG01515.hp2 HG01884.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.3266-174_3266-167d others(10): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517268 | ||||||
| chr3:129517268 | G | GCACACAC others(15): Show |
1 | a0001c0001t0001g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3266-188_3266-167d others(24): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517268 | ||||||
| chr3:129517268 | G | GCACGCAC others(3): Show |
1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3266-198_3266-197i others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517268 | ||||||
| chr3:129517268 | G | GCACGCGC others(5): Show |
1 | a0001c0003t0001g0270 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3266-198_3266-197i others(14): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517268 | ||||||
| chr3:129517268 | G | GCACGCGC others(7): Show |
3 | a0001c0003t0001g0269 a0001c0003t0001g0272 a0001c0003t0001g0273 |
3 | HG02572.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3266-198_3266-197i others(16): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517268 | ||||||
| chr3:129517268 | G | GCACGCGC others(11): Show |
2 | a0001c0003t0001g0271 a0001c0003t0001g0274 |
2 | HG02109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.3266-198_3266-197i others(20): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517268 | ||||||
| chr3:129517268 | GCA | G | 19 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0049 others(16): Show |
21 | HG01891.hp1 HG02074.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.3266-168_3266-167d others(4): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517268 | ||||||
| chr3:129517274 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.3266-195A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129517274 | |||||||
| chr3:129517276 | A | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
8 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.3266-193A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129517276 | |||||||
| chr3:129517293 | CACACACA others(3): Show |
C | 4 | a0001c0007t0001g0328 a0001c0007t0001g0329 a0001c0007t0001g0330 others(1): Show |
4 | HG01123.hp1 HG01175.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3266-174_3266-165d others(12): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517293 | ||||||
| chr3:129517297 | CACACAG | C | 28 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(25): Show |
33 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.3266-170_3266-165d others(8): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517297 | ||||||
| chr3:129517299 | CACAG | C | 4 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0004t0001g0021 others(1): Show |
5 | HG00735.hp1 HG00738.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3266-168_3266-165d others(6): Show |
IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr3 | 129517299 | ||||||
| chr3:129517303 | G | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
85 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.3266-166G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 26/29 | chr3 | 129517303 | |||||||
| chr3:129517680 | G | C | 1 | a0012c0017t0001g0114 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3391+86G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129517680 | |||||||
| chr3:129517736 | C | T | 2 | a0001c0009t0001g0099 a0001c0009t0001g0100 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3391+142C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129517736 | |||||||
| chr3:129517739 | A | G | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3391+145A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129517739 | |||||||
| chr3:129517893 | C | T | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3391+299C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129517893 | |||||||
| chr3:129517917 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG01884.hp1 HG02809.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3391+323T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129517917 | |||||||
| chr3:129517928 | C | T | 1 | a0001c0016t0001g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3391+334C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129517928 | |||||||
| chr3:129517942 | A | G | 1 | a0001c0003t0001g0271 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3391+348A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129517942 | |||||||
| chr3:129518101 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3391+507C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518101 | |||||||
| chr3:129518135 | G | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
20 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.3391+541G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518135 | |||||||
| chr3:129518136 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0281 a0001c0001t0001g0282 others(15): Show |
20 | HG01255.hp1 HG02055.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.3391+542C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518136 | |||||||
| chr3:129518167 | A | T | 1 | a0001c0016t0001g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3391+573A>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518167 | |||||||
| chr3:129518182 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3391+588C>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518182 | |||||||
| chr3:129518206 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | NA18957.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.3391+612C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518206 | |||||||
| chr3:129518252 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0153 |
4 | HG03139.hp2 NA18960.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.3391+658C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518252 | |||||||
| chr3:129518433 | T | G | 1 | a0001c0001t0001g0126 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3392-674T>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518433 | |||||||
| chr3:129518443 | T | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.3392-664T>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518443 | |||||||
| chr3:129518444 | C | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.3392-663C>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518444 | |||||||
| chr3:129518473 | C | T | 2 | a0002c0002t0001g0308 a0007c0014t0001g0314 |
2 | HG01168.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.3392-634C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518473 | |||||||
| chr3:129518535 | C | T | 1 | a0002c0002t0001g0318 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3392-572C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518535 | |||||||
| chr3:129518639 | T | C | 33 | a0001c0004t0001g0021 a0001c0004t0001g0322 a0001c0004t0001g0323 others(30): Show |
40 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.3392-468T>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518639 | |||||||
| chr3:129518705 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3392-402C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518705 | |||||||
| chr3:129518715 | G | T | 1 | a0001c0001t0001g0032 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3392-392G>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518715 | |||||||
| chr3:129518742 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
236 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.3392-365A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518742 | |||||||
| chr3:129518775 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0001g0116 |
4 | HG02258.hp2 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3392-332C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518775 | |||||||
| chr3:129518822 | C | T | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3392-285C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518822 | |||||||
| chr3:129518915 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3392-192A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 27/29 | chr3 | 129518915 | |||||||
| chr3:129519266 | G | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3471+80G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 28/29 | chr3 | 129519266 | |||||||
| chr3:129519292 | A | G | 1 | a0001c0004t0001g0327 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3471+106A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 28/29 | chr3 | 129519292 | |||||||
| chr3:129519397 | C | T | 1 | a0001c0004t0001g0326 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3472-171C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 28/29 | chr3 | 129519397 | |||||||
| chr3:129519438 | G | C | 1 | a0001c0001t0001g0081 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3472-130G>C | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 28/29 | chr3 | 129519438 | |||||||
| chr3:129519758 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3636+26A>G | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 29/29 | chr3 | 129519758 | |||||||
| chr3:129519922 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0160 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3636+190C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 29/29 | chr3 | 129519922 | |||||||
| chr3:129519962 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3637-214C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 29/29 | chr3 | 129519962 | |||||||
| chr3:129520010 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3637-166C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 29/29 | chr3 | 129520010 | |||||||
| chr3:129520086 | C | T | 1 | a0001c0008t0001g0068 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3637-90C>T | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 29/29 | chr3 | 129520086 | |||||||
| chr3:129520104 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3637-72G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 29/29 | chr3 | 129520104 | |||||||
| chr3:129520106 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3637-70G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 29/29 | chr3 | 129520106 | |||||||
| chr3:129520121 | G | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3637-55G>A | IFT122 | ENSG00000163913.14 | transcript | ENST00000348417.7 | protein_coding | 29/29 | chr3 | 129520121 |